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6 in total

1. Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy.

Authors: R C Hennekam; E G Renckens-Wennen
Journal: J Med Genet Date: 1990-10 Impact factor: 6.318

2. The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor.

Authors: G B Potter; G M Beaudoin; C L DeRenzo; J M Zarach; S H Chen; C C Thompson
Journal: Genes Dev Date: 2001-10-15 Impact factor: 11.361

3. Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias.

Authors: E Sprecher; R Bergman; R Szargel; R Friedman-Birnbaum; N Cohen
Journal: Am J Hum Genet Date: 1999-05 Impact factor: 11.025

4. Congenital universal alopecia, mental deficiency, and microcephaly in two sibs.

Authors: R A Pfeiffer; J Völklein
Journal: J Med Genet Date: 1982-10 Impact factor: 6.318

5. A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Authors: W Ahmad; A D Irvine; H Lam; C Buckley; E A Bingham; A A Panteleyev; M Ahmad; J A McGrath; A M Christiano
Journal: Am J Hum Genet Date: 1998-10 Impact factor: 11.025

Review 6. Hairless is a nuclear receptor corepressor essential for skin function.

Authors: Catherine C Thompson
Journal: Nucl Recept Signal Date: 2009-12-31

6 in total