(Q34737323)

4 August 2017

1 reference

title

Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: evidence from phenotypic evolution (English)

1 reference

4 August 2017

main subject

focal dermal hypoplasia

1 reference

Susan Hancock

1

1 reference

4 August 2017

Peter Pryde

2

1 reference

4 August 2017

Christine Fong

3

1 reference

4 August 2017

Jane E Brazy

4

1 reference

4 August 2017

Katharina Stewart

5

1 reference

4 August 2017

Amy Favour

6

1 reference

4 August 2017

Richard M Pauli

7

1 reference

4 August 2017

publication date

1 July 2002

1 reference

American Journal of Medical Genetics Part A

4 August 2017

published in

1 reference

4 August 2017

volume

110

1 reference

4 August 2017

issue

4

1 reference

4 August 2017

page(s)

370-379

1 reference

Focal dermal hypoplasia (Goltz's syndrome).

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Focal dermal hypoplasia syndrome. Case report and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin Syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Focal dermal hypoplasia (Goltz syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

A case of focal dermal hypoplasia syndrome (Goltz) with bilateral cheilo-gnatho-palatoschisis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

New multiple congenital anomalies syndrome in a stillborn infant of consanguinous parents and a prediabetic pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Variable expression in focal dermal hypoplasia. An example of differential X-chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

Focal dermal hypoplasia (Goltz syndrome) presenting as a severe fetal malformation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10456

21 January 2018

Identifiers

DOI

10.1002/AJMG.10456

1 reference

4 August 2017

1 reference