(Q28254095)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

review article

1 reference

title

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Lisa J Kobrynski

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

English

0 references

publication date

1 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

370

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

9596

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

1443-1452

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

9 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Prevalence of 22q11 microdeletion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

A population study of chromosome 22q11 deletions in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

DiGeorge syndrome: part of CATCH 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

The annual incidence of DiGeorge/velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Differential detection of deletion 22q11.2 syndrome by specialty and indication.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Familial deletions of chromosome 22q11

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Computational analysis and refinement of sequence structure on chromosome 22q11.2 region: application to the development of quantitative real-time PCR assay for clinical diagnosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Role of TBX1 in human del22q11.2 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Coincident DiGeorge anomaly and renal agenesis and its relation to maternal diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Maternal diabetes causing DiGeorge anomaly and renal agenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Immune deficiency in CHARGE association

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

[Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2]

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

22q11 deletions in patients with conotruncal heart defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Chromosome 22q11 deletions in patients with conotruncal heart defects

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Accuracy in identification of patients with 22q11.2 deletion by likely care providers using facial photographs.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

The DNA sequence of human chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Association of 22q11 deletion with isolated congenital heart disease in three Chinese ethnic groups.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Isl1 is upstream of sonic hedgehog in a pathway required for cardiac morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Isl1Cre reveals a common Bmp pathway in heart and limb development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Tbx1 is regulated by forkhead proteins in the secondary heart field

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Fgf8 is required for anterior heart field development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Developmental expression of the amphioxus Tbx1/ 10 gene illuminates the evolution of vertebrate branchial arches and sclerotome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Retinoic acid down-regulates Tbx1 expression in vivo and in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Genetic Syndromes and Outcome After Surgical Correction of Tetralogy of Fallot

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Long-term assessment of T-cell populations in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

A new concept of the cellular basis of immunity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Lack of Correlation between Impaired T Cell Production, Immunodeficiency, and Other Phenotypic Features in Chromosome 22q11.2 Deletion Syndromes (DiGeorge Syndrome/Velocardiofacial Syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Possible extrathymic development of nonfunctional T cells in a patient with complete DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Maldescent of the thymus: 34 necropsy and 10 surgical cases, including 7 thymuses medial to the mandible

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Retropharyngeal aberrant thymus.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

DiGeorge anomaly: a comparative study of the clinical and immunologic characteristics of patients positive and negative by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Maturational alterations of peripheral T cell subsets and cytokine gene expression in 22q11.2 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Humoral immunity in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Prediction of persistent immunodeficiency in the DiGeorge anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Post-Natal Ontogenesis of the T-Cell Receptor CD4 and CD8 Vβ Repertoire and Immune Function in Children with DiGeorge Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (digeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Safety and immunogenicity of measles–mumps–rubella vaccine in children with congenital immunodeficiency (DiGeorge syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Immune constitution of complete DiGeorge anomaly by transplantation of unmobilised blood mononuclear cells

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Bone marrow transplantation in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Transplantation of thymus tissue in complete DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Visual function in velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

An outcome evaluation of sphincter pharyngoplasty for the management of velopharyngeal insufficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Surgical correction of velopharyngeal insufficiency in children with velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Communication issues in 22q11.2 deletion syndrome: children at risk.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Communication disorders in the 22Q11.2 microdeletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Chromosome 22q11.2 deletion syndrome: an underestimated cause of neuropsychiatric impairment in adolescence

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Attention deficits in children with 22q.11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2807%2961601-8

7 January 2021

10.1016/S0140-6736(07)61601-8

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17950858%20AND%20SRC:MED&resulttype=core&format=json