(Q38735488)

6 September 2017

1 reference

title

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

1 reference

6 September 2017

1 reference

Cohen MM Jr

1

1 reference

6 September 2017

publication date

1 September 1989

1 reference

Birth Defects Research Part A: Clinical and Molecular Teratology

6 September 2017

published in

1 reference

6 September 2017

volume

40

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6 September 2017

issue

3

1 reference

6 September 2017

page(s)

211-235

1 reference

The "D" syndrome. Report of four trisomic and one D/D translocation case.

6 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FTERA.1420400304

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FTERA.1420400304

Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FTERA.1420400304

Campomelic dysplasia. Further elucidation of a distinct entity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FTERA.1420400304

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%2FTERA.1420400304

21 January 2018

Identifiers

DOI

10.1002/TERA.1420400304

1 reference

6 September 2017

1 reference