Clinical, genetic and environmental factors associated with congenital vertebral malformations (Q36802361)

16 August 2017

Clinical, genetic and environmental factors associated with congenital vertebral malformations (English)

1 reference

16 August 2017

0 references

C McCarty

0 references

P F Giampietro

1 reference

16 August 2017

C L Raggio

1 reference

16 August 2017

R D Blank

1 reference

16 August 2017

U Broeckel

1 reference

16 August 2017

M A Pickart

1 reference

16 August 2017

1 February 2013

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16 August 2017

Molecular syndromology

1 reference

16 August 2017

1 reference

16 August 2017

1-2

1 reference

16 August 2017

94-105

1 reference

Molecular diagnosis of vertebral segmentation disorders in humans

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Role of Chd7 in zebrafish: a model for CHARGE syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Human genome sequencing in health and disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Wildervanck's syndrome and mirror movements: a congenital disorder of axon migration?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Chd7 plays a critical role in controlling left-right symmetry during zebrafish somitogenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Complications of growth-sparing surgery in early onset scoliosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

The world of twins: an update.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Hyperthermia: malformations to chaperones

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Role of environmental factors in axial skeletal dysmorphogenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Congenital scoliosis in monozygotic twins: case report and review of possible factors contributing to its development

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

A missense T (Brachyury) mutation contributes to vertebral malformations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Maternal methyl supplements increase offspring DNA methylation at Axin Fused

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

An analysis of PAX1 in the development of vertebral malformations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutated MESP2 causes spondylocostal dysostosis in humans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Epigenetics and assisted reproductive technology: a call for investigation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Idiopathic scoliosis in families of children with congenital scoliosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Investigations into the association between cervicomedullary neuroschisis and mirror movements in patients with Klippel-Feil syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

A genetic study of the human T gene and its exclusion as a major candidate gene for sacral agenesis with anorectal atresia.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Teratogenic effects of sodium valproate in mice and rats at midgestation and at term

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Multiple vertebral segmentation defects: analysis of 26 new patients and review of the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Persistent mirror movements: a clinical study of 17 children, adolescents and young adults

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Spondylothoracic dysplasia--a syndrome of congenital anomalies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Retinoic acid embryopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Oculoauriculovertebral spectrum: an updated critique

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Heat shock during rat embryo development in vitro results in decreased mitosis and abundant cell death.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Cervical spine anomalies in fetal alcohol syndrome.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Phenytoin teratogenicity in man.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Teratogenicity and developmental toxicity of valproic acid in rats

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Klippel-Feil syndrome, iniencephalus, anencephalus, hindbrain hernia and mirror movements: overdistention of the neural tube

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Fetal Skeletal Malformations Associated with Moderate Zinc Deficiency During Pregnancy

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

A mechanism for gene-environment interaction in the etiology of congenital scoliosis.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Complications of growing-rod treatment for early-onset scoliosis: analysis of one hundred and forty patients.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Pilot assessment of a radiologic classification system for segmentation defects of the vertebrae.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Effects of retinoic acid on Dominant hemimelia expression in mice

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Pulmonary function following early thoracic fusion in non-neuromuscular scoliosis

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Teratogenicity and developmental toxicity of chlorpyrifos. Maternal exposure during organogenesis in mice

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Defects in cervical vertebrae in boric acid-exposed rat embryos are associated with anterior shifts of hox gene expression domains

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

The characteristics of thoracic insufficiency syndrome associated with fused ribs and congenital scoliosis.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Infants of diabetic mothers are at increased risk for the oculo-auriculo-vertebral sequence: A case-based and case-control approach

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Validity of the Hfm transgenic mouse as a model for hemifacial microsomia.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Stage-specific skeletal and visceral defects of the I(Kr)-blocker almokalant: further evidence for teratogenicity via a hypoxia-related mechanism

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mouse model for thoracic congenital scoliosis.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

The teratogenicity of anticonvulsant drugs

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Cervical disc prolapse in childhood associated with Klippel-Feil syndrome.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Epidemiological analysis of outcomes of pregnancy in gestational diabetic mothers

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Klippel-Feil syndrome: CT and MR of acquired and congenital abnormalities of cervical spine and cord.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Mirror movements in patients with the Klippel-Feil syndrome. Neuropathologic observations

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Scoliosis and congenital anomalies associated with Klippel-Feil syndrome types I-III

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638777

Congenital malformations among infants whose mothers had gestational diabetes or preexisting diabetes

20 October 2018

1 reference

12 December 2020

The Natural History of Klippel-Feil Syndrome: Clinical, Roentgenographic, and Magnetic Resonance Imaging Findings at Adulthood

1 reference

12 December 2020

Ultrastructural changes in 9-day old mouse embryos following maternal tobacco smoke inhalation

1 reference

12 December 2020

Syndrome of caudal regression in infants of diabetic mothers: observations of further cases

1 reference

12 December 2020

A retrospective cohort study of pulmonary function, radiographic measures, and quality of life in children with congenital scoliosis: an evaluation of patient outcomes after early spinal fusion

1 reference

12 December 2020

Role of nitric oxide in chick embryonic organogenesis and dysmorphogenesis

1 reference

12 December 2020

Spine and rib abnormalities and stature in spondylocostal dysostosis

1 reference

12 December 2020

DLL3 as a candidate gene for vertebral malformations

1 reference

12 December 2020

Examination of the newborn with congenital scoliosis: focus on the physical

1 reference

12 December 2020

Evaluation of SLC35A3 as a candidate gene for human vertebral malformations

1 reference

12 December 2020

Racial/ethnic differences in smoking, other risk factors, and low birth weight among low-income pregnant women, 1978-1988

1 reference

12 December 2020

A clock and wavefront model for control of the number of repeated structures during animal morphogenesis

1 reference

12 December 2020

Sublethal effects of tetrachloro-1,2-benzoquinone—A component in bleachery effluents from pulp mills—On vertebral quality and physiological parameters in fourhorn sculpin

1 reference

12 December 2020

Array-CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum

1 reference

12 December 2020

The natural history of congenital scoliosis. A study of two hundred and fifty-one patients

1 reference

12 December 2020

The incidence of limb and ear defects since the withdrawal of thalidomide

1 reference

12 December 2020

Identifiers

DOI

10.1159/000345329

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23653580

1 reference