(Q48939764)

17 February 2018

title

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3). (English)

1 reference

17 February 2018

1 reference

Estabrooks LL

1

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17 February 2018

Rao KW

series ordinal

2

1 reference

17 February 2018

Donahue RP

series ordinal

3

1 reference

17 February 2018

Aylsworth AS

series ordinal

4

1 reference

17 February 2018

publication date

1 July 1990

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17 February 2018

American Journal of Medical Genetics Part A

published in

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17 February 2018

volume

36

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17 February 2018

page(s)

306-309

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17 February 2018

issue

3

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17 February 2018

An update on the holoprosencephalic disorders.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

Chance vs. causality in the association of Down syndrome and holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

Roentgenology of holoprosencephaly (arhinencephaly).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

Holoprosencephaly in a Down syndrome child

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.1320360312

21 January 2018

Identifiers

DOI

10.1002/AJMG.1320360312

1 reference

17 February 2018

PubMed ID

2363428

1 reference

17 February 2018