(Q36604059)

English

Holoprosencephaly: clinical, anatomic, and molecular dimensions

scientific article published on September 2006

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Europe PubMed Central

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15 August 2017

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Europe PubMed Central

title

Holoprosencephaly: clinical, anatomic, and molecular dimensions (English)

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Europe PubMed Central

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15 August 2017

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M Michael Cohen

1

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17001700

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15 August 2017

publication date

1 September 2006

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15 August 2017

published in

Birth Defects Research Part A: Clinical and Molecular Teratology

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17001700

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15 August 2017

volume

76

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issue

9

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15 August 2017

page(s)

658-673

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15 August 2017

cites work

Midline cerebral dysgenesis, dysfunction of the hypothalamic-pituitary axis, and fetal alcohol effects

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FBDRA.20295

retrieved

21 January 2018

FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP AND PALATE. REPORT OF PATIENT WITH 46 CHROMOSOMES.

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https://api.crossref.org/works/10.1002%2FBDRA.20295

retrieved

21 January 2018

Absence of the superior labial frenulum in holoprosencephaly: a new diagnostic sign.

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https://api.crossref.org/works/10.1002%2FBDRA.20295

retrieved

21 January 2018

Holoprosencephaly with median cleft lip. Clinical, pathological, and echoencephalographic study.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FBDRA.20295

retrieved

21 January 2018

Identifiers

DOI

10.1002/BDRA.20295

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17001700

retrieved

15 August 2017

PubMed publication ID

17001700

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17001700

retrieved

15 August 2017

(Q36604059)

Holoprosencephaly: clinical, anatomic, and molecular dimensions

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