Literature DB >> 15200512

Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.

M A Rafiq1, M Ansar, T Pham, M Amin-ud-Din, M Anwar, S Haque, M H Chahrour, K Yan, S M Leal, W Ahmad.   

Abstract

We report on a six-generation Pakistani consanguineous family with autosomal recessive transmission of a form of hereditary nail dysplasia. Affected individuals presented with onycholysis of fingernails and anonychia of toenails. Associated abnormalities of ectodermal appendages were not observed in any of the affected individuals. Linkage has been established to chromosome 17q. A maximum multipoint analysis logarithm of the odds ratio score of 4.85 was obtained at marker D17S1301. Due to the consanguineous nature of this kindred, the gene for nail dysplasia is probably contained within a 5.0-cM (3 MB on the sequence-based physical map) region of homozygosity flanked by markers D17S1807 and D17S937.

Entities:  

Mesh:

Year:  2004        PMID: 15200512      PMCID: PMC6141021          DOI: 10.1111/j.0009-9163.2004.00273.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  19 in total

1.  Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics.

Authors:  E Sobel; K Lange
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.

Authors:  S D Dreyer; G Zhou; A Baldini; A Winterpacht; B Zabel; W Cole; R L Johnson; B Lee
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

3.  X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.

Authors:  N S Heiss; S W Knight; T J Vulliamy; S M Klauck; S Wiemann; P J Mason; A Poustka; I Dokal
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

4.  Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.

Authors:  H Chen; Y Lun; D Ovchinnikov; H Kokubo; K C Oberg; C V Pepicelli; L Gan; B Lee; R L Johnson
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

5.  Computer programs for multilocus haplotyping of general pedigrees.

Authors:  D E Weeks; E Sobel; J R O'Connell; K Lange
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

6.  Hereditary twenty-nail dystrophy in a Sicilian family.

Authors:  L Pavone; S Li Volti; B Guarneri; M La Rosa; G Sorge; G Incorpora; F Mollica
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

7.  Isolated congenital nail dysplasia: a new autosomal dominant condition.

Authors:  H Hamm; S Karl; E B Bröcker
Journal:  Arch Dermatol       Date:  2000-10

8.  Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Authors:  K W Broman; J C Murray; V C Sheffield; R L White; J L Weber
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

9.  Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia.

Authors:  F Vidal; D Aberdam; C Miquel; A M Christiano; L Pulkkinen; J Uitto; J P Ortonne; G Meneguzzi
Journal:  Nat Genet       Date:  1995-06       Impact factor: 38.330

10.  Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25.

Authors:  C Ruhrberg; J A Williamson; D Sheer; F M Watt
Journal:  Genomics       Date:  1996-11-01       Impact factor: 5.736

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.