(Q47636876)

4 February 2018

title

Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989. (English)

1 reference

4 February 2018

0 references

1 reference

Olsen CL

1

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4 February 2018

Hughes JP

series ordinal

2

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4 February 2018

Youngblood LG

series ordinal

3

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4 February 2018

Sharpe-Stimac M

series ordinal

4

1 reference

4 February 2018

publication date

1 December 1997

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4 February 2018

American Journal of Medical Genetics Part A

published in

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4 February 2018

volume

73

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4 February 2018

issue

2

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4 February 2018

page(s)

217-226

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4 February 2018

Cyclopia and congenital cytomegalovirus infection.

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Holoprosencephaly: epidemiologic and clinical characteristics of a California population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Congenital malformations in newborns of women with established and gestational diabetes in Washington State, 1984-91.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Holoprosencephaly and related midline cerebral anomalies: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Cytogenetic variants in holoprosencephaly. Report of a case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Mediobasal prosencephalic defects, including holoprosencephaly and cyclopia, in relation to the development of the human forebrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

The oral manifestations of cyclopia. Review of the literature and report of two cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C217%3A%3AAID-AJMG20%3E3.0.CO%3B2-S

10.1002/(SICI)1096-8628(19971212)73:2<217::AID-AJMG20>3.0.CO;2-S

21 January 2018

Identifiers

DOI

1 reference

4 February 2018

PubMed ID

9409876

1 reference

4 February 2018