Literature DB >> 15520410

A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3.

M Aslam, M H Chahrour, A Razzaq, S Haque, K Yan, S M Leal, W Ahmad.   

Abstract

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Year:  2004        PMID： 15520410      PMCID： PMC1735610          DOI： 10.1136/jmg.2004.019729

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  9 in total

1.  Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3.

Authors:  Peter John; Ghazanfar Ali; Muhammad S Chishti; Syed Muhammad S Naqvi; Suzanne M Leal; Wasim Ahmad
Journal:  Hum Genet       Date:  2005-11-05       Impact factor: 4.132

2.  Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genes.

Authors:  Sulman Basit; Ghazanfar Ali; Naveed Wasif; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-06-11       Impact factor: 4.132

3.  A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.

Authors:  A Wali; P John; A Gul; K Lee; M S Chishti; G Ali; M J Hassan; S M Leal; W Ahmad
Journal:  Clin Genet       Date:  2006-09       Impact factor: 4.438

4.  A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis.

Authors:  Ghazanfar Ali; Muhammad Salman Chishti; Syed Irfan Raza; Peter John; Wasim Ahmad
Journal:  Hum Genet       Date:  2007-02-27       Impact factor: 4.132

5.  Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.

Authors:  Gul Naz; Ghazanfar Ali; Syed Kamran-ul-Hassan Naqvi; Zahid Azeem; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

6.  Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.

Authors:  A Wali; G Ali; P John; K Lee; M S Chishti; S M Leal; W Ahmad
Journal:  Ann Hum Genet       Date:  2007-04-19       Impact factor: 1.670

7.  Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).

Authors:  Zahid Azeem; Musharraf Jelani; Gul Naz; Muhammad Tariq; Naveed Wasif; Syed Kamran-Ul-Hassan Naqvi; Muhammad Ayub; Masoom Yasinzai; Muhammad Amin-Ud-Din; Abdul Wali; Ghazanfar Ali; Muhammad Salman Chishti; Wasim Ahmad
Journal:  Hum Genet       Date:  2008-05-07       Impact factor: 4.132

8.  Genetic dissection of two Pakistani families with consanguineous localized autosomal recessive hypotrichosis (LAH).

Authors:  Seyyedha Abbas; Abdul Khaliq Naveed; Shakir Khan; Muhammad Jawad Yousaf; Zahid Azeem; Suhail Razak; Fatima Qaiser
Journal:  Iran J Basic Med Sci       Date:  2014-07       Impact factor: 2.699

9.  A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair.

Authors:  Muhammad Tariq; Aysha Azhar; Shahid Mahmood Baig; Niklas Dahl; Joakim Klar
Journal:  Sci Rep       Date:  2012-10-12       Impact factor: 4.379
  9 in total

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