127 related articles for article (PubMed ID: 19751230)
1. A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12 approximately 12.3 in a Chinese family.
Xu C; Zhang L; Chen N; Su B; Pan CM; Li JY; Zhang GW; Liu Z; Sheng Y; Song HD
J Cutan Pathol; 2010 Jul; 37(7):758-63. PubMed ID: 19751230
[TBL] [Abstract][Full Text] [Related]
2. An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family.
Baumer A; Belli S; Trüeb RM; Schinzel A
Eur J Hum Genet; 2000 Jun; 8(6):443-8. PubMed ID: 10878665
[TBL] [Abstract][Full Text] [Related]
3. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
Wali A; Chishti M; Ayub M; Yasinzai M; Kafaitullah ; Ali G; John P; Ahmad W
Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
[TBL] [Abstract][Full Text] [Related]
4. A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
Betz RC; Lee YA; Bygum A; Brandrup F; Bernal AI; Toribio J; Alvarez JI; Kukuk GM; Ibsen HH; Rasmussen HB; Wienker TF; Reis A; Propping P; Kruse R; Cichon S; Nöthen MM
Am J Hum Genet; 2000 Jun; 66(6):1979-83. PubMed ID: 10793007
[TBL] [Abstract][Full Text] [Related]
5. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
He PP; Zhang XJ; Yang Q; Li M; Liang YH; Yang S; Yan KL; Cui Y; Shen YY; Wang HY; Sun LD; Du WH; Shen YJ; Xu SJ; Huang W
Br J Dermatol; 2004 May; 150(5):837-42. PubMed ID: 15149494
[TBL] [Abstract][Full Text] [Related]
6. Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.
Naz G; Ali G; Naqvi SK; Azeem Z; Ahmad W
Hum Genet; 2010 Apr; 127(4):395-401. PubMed ID: 20054564
[TBL] [Abstract][Full Text] [Related]
7. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.
Yang S; Gao M; Cui Y; Yan KL; Ren YQ; Zhang GL; Wang PG; Xiao FL; Du WH; Liang YH; Sun LD; Xu SJ; Huang W; Zhang XJ
J Invest Dermatol; 2005 Oct; 125(4):711-4. PubMed ID: 16185270
[TBL] [Abstract][Full Text] [Related]
8. Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genes.
Basit S; Ali G; Wasif N; Ansar M; Ahmad W
Hum Genet; 2010 Aug; 128(2):213-20. PubMed ID: 20544222
[TBL] [Abstract][Full Text] [Related]
9. A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.
Rafique MA; Ansar M; Jamal SM; Malik S; Sohail M; Faiyaz-Ul-Haque M; Haque S; Leal SM; Ahmad W
Eur J Hum Genet; 2003 Aug; 11(8):623-8. PubMed ID: 12891384
[TBL] [Abstract][Full Text] [Related]
10. Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family.
Ma JH; Shen SH; Zhang GW; Zhao DS; Xu C; Pan CM; Jiang H; Wang ZQ; Song HD
Mol Vis; 2010 Oct; 16():2043-54. PubMed ID: 21042559
[TBL] [Abstract][Full Text] [Related]
11. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.
Basit S; Wali A; Aziz A; Muhammad N; Jelani M; Ahmad W
Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890
[TBL] [Abstract][Full Text] [Related]
12. Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.
Mir A; Ansar M; Chahrour MH; Pham TL; Wajid M; Haque S; Yan K; Ahmad W; Leal SM
Am J Med Genet A; 2005 Feb; 133A(1):23-6. PubMed ID: 15637723
[TBL] [Abstract][Full Text] [Related]
13. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
Cichon S; Kruse R; Hillmer AM; Kukuk G; Anker M; Altland K; Knapp M; Propping P; Nöthen MM
Br J Dermatol; 2000 Oct; 143(4):811-4. PubMed ID: 11069461
[TBL] [Abstract][Full Text] [Related]
14. A new locus for autosomal dominant congenital coronary cataract in a Chinese family maps to chromosome 3q.
Liu G; Li Y; Ruan Y; Cao W; Xin L; Qian J; Gu J
Mol Vis; 2010 May; 16():874-9. PubMed ID: 20508730
[TBL] [Abstract][Full Text] [Related]
15. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
Lefevre P; Rochat A; Bodemer C; Vabres P; Barrandon Y; de Prost Y; Garner C; Hovnanian A
Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110
[TBL] [Abstract][Full Text] [Related]
16. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.
van Steensel M; Smith FJ; Steijlen PM; Kluijt I; Stevens HP; Messenger A; Kremer H; Dunnill MG; Kennedy C; Munro CS; Doherty VR; McGrath JA; Covello SP; Coleman CM; Uitto J; McLean WH
Am J Hum Genet; 1999 Aug; 65(2):413-9. PubMed ID: 10417283
[TBL] [Abstract][Full Text] [Related]
17. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G
Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197
[TBL] [Abstract][Full Text] [Related]
18. A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2.
Leal GF; Roberts E; Silva EO; Costa SM; Hampshire DJ; Woods CG
J Med Genet; 2003 Jul; 40(7):540-2. PubMed ID: 12843329
[No Abstract] [Full Text] [Related]
19. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
Yuan Y; Zhou X; Wang F; Yan M; Ding F
Curr Eye Res; 2011 Feb; 36(2):154-67. PubMed ID: 21281067
[TBL] [Abstract][Full Text] [Related]
20. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
Wang L; Lin H; Shen Y; Huang S; Gu J; Su H; Qi Y
Mol Vis; 2007 Aug; 13():1357-62. PubMed ID: 17768382
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]