Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: Possible association with Beckwith-Wiedemann syndrome (Q67931444)

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scientific article published on 01 June 1991

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English	Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: Possible association with Beckwith-Wiedemann syndrome	scientific article published on 01 June 1991

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1864589%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: possible association with Beckwith-Wiedemann syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1864589%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: Possible association with Beckwith-Wiedemann syndrome (English)

1 reference

10.1016/0046-8177(91)90237-J

https://api.crossref.org/works/10.1016/0046-8177(91)90237-J

12 December 2022

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

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author name string

J. M. Lage

1

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Europe PubMed Central

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12 December 2022

language of work or name

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National Center for Biotechnology Information

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1864589

12 December 2022

publication date

1 June 1991

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19 September 2019

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10.1016/0046-8177(91)90237-J

https://api.crossref.org/works/10.1016/0046-8177(91)90237-J

12 December 2022

https://api.elsevier.com/content/article/PII:004681779190237J?httpAccept=text/plain

1 reference

10.1016/0046-8177(91)90237-J

https://api.crossref.org/works/10.1016/0046-8177(91)90237-J

12 December 2022

Human Pathology

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Europe PubMed Central

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19 September 2019

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19 September 2019

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19 September 2019

591-597

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1864589%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Hydatidiform mole: two entities. A morphologic and cytogenetic study with some clinical consideration

1

1 reference

10.1016/0046-8177(91)90237-J

https://api.crossref.org/works/10.1016/0046-8177(91)90237-J

12 December 2022

The syndromes of hydatidiform mole. I. Cytogenetic and morphologic correlations

2

1 reference

10.1016/0046-8177(91)90237-J

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12 December 2022

The syndromes of hydatidiform mole. II. Morphologic evolution of the complete and partial mole

3

1 reference

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Complete and partial hydatidiform mole in Hawaii: cytogenetics, morphology and epidemiology

4

1 reference

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12 December 2022

The clinicopathologic profile of the partial hydatidiform mole

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1 reference

10.1016/0046-8177(91)90237-J

https://api.crossref.org/works/10.1016/0046-8177(91)90237-J

12 December 2022

Cytogenetic and clinicopathologic studies of partial moles

7

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10.1016/0046-8177(91)90237-J

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12 December 2022

The syndrome of partial mole

8

1 reference

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12 December 2022

Genetic studies on hydatidiform moles. I. The origin of partial moles

9

1 reference

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12 December 2022

Androgenetic origin of hydatidiform mole

10

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10.1016/0046-8177(91)90237-J

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12 December 2022

Hydrops fetalis

11

1 reference

10.1016/0046-8177(91)90237-J

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12 December 2022

Differential diagnosis of hydrops fetalis

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1 reference

10.1016/0046-8177(91)90237-J

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12 December 2022

Hydrops revisited: literature review of 1,414 cases published in the 1980s

14

1 reference

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12 December 2022

New syndrome of neonatal hypoglycemia. Association with visceromegaly, macroglossia, microcephaly and abnormal umbilicus

19

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12 December 2022

Exomphalos with macroglossia: a study of eleven cases.

20

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Hydatidiform moles. Application of flow cytometry in diagnosis

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12 December 2022

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

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1 reference

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12 December 2022

The placenta in familial beckwith-wiedemann syndrome

23

1 reference

10.1016/0046-8177(91)90237-J

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12 December 2022

Abnormally large placenta associated with Beckwith-Wiedemann syndrome

24

1 reference

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12 December 2022

Prenatal ultrasound diagnosis of macroglossia in the Wiedemann-Beckwith syndrome

26

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In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case report

27

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The Beckwith-Wiedemann syndrome. Seven new cases

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12 December 2022

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

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Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

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Development of homozygosity for chromosome 11p markers in Wilms' tumour

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Loss of a Harvey ras allele in sporadic Wilms' tumour

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Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

34

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12 December 2022

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

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The clinical syndrome of triploidy

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Morphologic anomalies in triploid liveborn fetuses

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Fetal omphalocele: associated malformations and chromosomal defects

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Fetomaternal hemorrhage associated with umbilical vein thrombosis. Case report

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Ultrasound demonstration of masses in a 15 week fetus: hydrops in a fetus with umbilical cord occlusion

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12 December 2022

Identifiers

10.1016/0046-8177(91)90237-J

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1864589%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1864589%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

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