(Q40745188)

23 September 2017

Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome (English)

1 reference

23 September 2017

1 reference

Wessagowit V

1

1 reference

23 September 2017

Mellerio JE

series ordinal

2

1 reference

23 September 2017

Pembroke AC

series ordinal

3

1 reference

23 September 2017

McGrath JA

series ordinal

4

1 reference

23 September 2017

1 July 2000

1 reference

Clinical and Experimental Dermatology

23 September 2017

1 reference

23 September 2017

25

1 reference

23 September 2017

441-443

1 reference

23 September 2017

5

1 reference

p63 is a p53 homologue required for limb and epidermal morphogenesis

23 September 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2000.00683.X

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2000.00683.X

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2000.00683.X

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2000.00683.X

Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2230.2000.00683.X

10.1046/J.1365-2230.2000.00683.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference