Literature DB >> 8252033

Homozygosity mapping: familiarity breeds debility.

M Farrall.   

Abstract

Mesh：

Year:  1993        PMID： 8252033     DOI： 10.1038/ng1093-107

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  9 in total

1.  A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters.

Authors:  A Ruiz; S Borrego; I Marcos; G Antiñolo
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

2.  Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

Authors:  E N Levy; Y Shen; A Kupelian; L Kruglyak; I Aksentijevich; E Pras; J E Balow; B Linzer; X Chen; D A Shelton; D Gumucio; M Pras; M Shohat; J I Rotter; N Fischel-Ghodsian; R I Richards; D L Kastner
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

3.  Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

Authors:  L Kruglyak; M J Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

4.  Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

Authors:  J P Rubio; A Danek; C Stone; R Chalmers; N Wood; C Verellen; X Ferrer; A Malandrini; G M Fabrizi; M Manfredi; J Vance; M Pericak-Vance; R Brown; G Rudolf; F Picard; E Alonso; M Brin; A H Németh; M Farrall; A P Monaco
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

5.  Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa.

Authors:  Kota Lalitha; Subhadra Jalali; Tejas Kadakia; Chitra Kannabiran
Journal:  J Genet       Date:  2002-08       Impact factor: 1.166

6.  The profile of major congenital abnormalities in the United Arab Emirates (UAE) population.

Authors:  L I al-Gazali; A H Dawodu; K Sabarinathan; M Varghese
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

7.  Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.

Authors:  P M Thomas; G J Cote; D M Hallman; P M Mathew
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

8.  Homozygosity for a new mutation (Ile119-->Met) in the insulin receptor gene in five sibs with familial insulin resistance.

Authors:  J Hone; D Accili; L I al-Gazali; G Lestringant; T Orban; S I Taylor
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

9.  The Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9.

Authors:  Jesús Aguirre-Hernández; Kaisa Wickström; David R Sargan
Journal:  BMC Vet Res       Date:  2007-07-10       Impact factor: 2.741
  9 in total

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