Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.

Author:

Kabbaj K,Baala L,Chhoul H,Sefiani A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia;Clarke, A.; Philips, D.I.M.; Brown, R.; Harper, P.S.;Arch Dis Child,1987

2. Two cases in which the skin and teeth were;Thurnam, J.

3. The variation of animals and plants under domestication;Darwin, C.

4. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes;McKusick, V.A.,1994

5. 1 st international workshop on human gene mapping;Gerald, P.S.; Brown, J.A.;Cytogenet Cell Genet,1974

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Autosomal recessive anhidrotic ectodermal dysplasia: A rare entity;Indian Journal of Dermatology;2014

2. Hypohidrotic (anhidrotic) ectodermal dysplasia in female twins;Nigerian Journal of Clinical Practice;2012

3. Genetic Disorders in Morocco;Genetic Disorders Among Arab Populations;2010

4. Dental agenesis: genetic and clinical perspectives;Journal of Oral Pathology & Medicine;2008-09-03

5. Les signes dermatologiques de la dysplasie ectodermique anhidrotique;Annales de Dermatologie et de Vénéréologie;2004-01

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