156 related articles for article (PubMed ID: 10909853)
21. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Masmoudi S; Charfedine I; Rebeh IB; Rebai A; Tlili A; Ghorbel AM; Belguith H; Petit C; Drira M; Ayadi H
Clin Genet; 2004 Oct; 66(4):358-64. PubMed ID: 15355440
[TBL] [Abstract][Full Text] [Related]
22. Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
Eisenberg I; Hochner H; Shemesh M; Levi T; Potikha T; Sadeh M; Argov Z; Jackson CL; Mitrani-Rosenbaum S
Eur J Hum Genet; 2001 Jul; 9(7):501-9. PubMed ID: 11464241
[TBL] [Abstract][Full Text] [Related]
23. Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy).
Asaka T; Ikeuchi K; Okino S; Takizawa Y; Satake R; Nitta E; Komai K; Endo K; Higuchi S; Oyake T; Yoshimura T; Suenaga A; Uyama E; Saito T; Konagaya M; Sunohara N; Namba R; Takada H; Honke K; Nishina M; Tanaka H; Shinagawa M; Tanaka K; Matsushima A; Tsuji S; Takamori M
J Hum Genet; 2001; 46(11):649-55. PubMed ID: 11721884
[TBL] [Abstract][Full Text] [Related]
24. Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13.
Martin N; Jaubert J; Glaser P; Szatanik M; Guénet JL
Genomics; 2001 Jul; 75(1-3):9-16. PubMed ID: 11472062
[TBL] [Abstract][Full Text] [Related]
25. Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
Viollet L; Zarhrate M; Maystadt I; Estournet-Mathiaut B; Barois A; Desguerre I; Mayer M; Chabrol B; LeHeup B; Cusin V; Billette De Villemeur T; Bonneau D; Saugier-Veber P; Touzery-De Villepin A; Delaubier A; Kaplan J; Jeanpierre M; Feingold J; Munnich A
Eur J Hum Genet; 2004 Jun; 12(6):483-8. PubMed ID: 15054395
[TBL] [Abstract][Full Text] [Related]
26. [Gene mapping of a nonsyndromic hearing impairmint family].
Cheng L; Gong Y; Liu Q; Chen B; Guo C; Li J; Zhang X; Lu Y; Gao G; Zhou H; Guo Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):89-93. PubMed ID: 12673573
[TBL] [Abstract][Full Text] [Related]
27. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
[TBL] [Abstract][Full Text] [Related]
28. Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.
Abu A; Frydman M; Marek D; Pras E; Stolovitch C; Aviram-Goldring A; Rienstein S; Reznik-Wolf H; Pras E
Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5283-7. PubMed ID: 17122114
[TBL] [Abstract][Full Text] [Related]
29. Clinical, pathological and molecular findings in two siblings with giant axonal neuropathy (GAN): report from India.
Nalini A; Gayathri N; Yasha TC; Ravishankar S; Urtizberea A; Huehne K; Rautenstrauss B
Eur J Med Genet; 2008; 51(5):426-35. PubMed ID: 18595793
[TBL] [Abstract][Full Text] [Related]
30. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
Mustapha M; Chouery E; Chardenoux S; Naboulsi M; Paronnaud J; Lemainque A; Mégarbané A; Loiselet J; Weil D; Lathrop M; Petit C
Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
[TBL] [Abstract][Full Text] [Related]
31. Giant axonal neuropathy: clinical and genetic study in six cases.
Demir E; Bomont P; Erdem S; Cavalier L; Demirci M; Kose G; Muftuoglu S; Cakar AN; Tan E; Aysun S; Topcu M; Guicheney P; Koenig M; Topaloglu H
J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):825-32. PubMed ID: 15897506
[TBL] [Abstract][Full Text] [Related]
32. Efficient construction of a physical map by fiber-FISH of the CLN5 region: refined assignment and long-range contig covering the critical region on 13q22.
Klockars T; Savukoski M; Isosomppi J; Laan M; Järvelä I; Petrukhin K; Palotie A; Peltonen L
Genomics; 1996 Jul; 35(1):71-8. PubMed ID: 8661106
[TBL] [Abstract][Full Text] [Related]
33. Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysis.
Giehl KA; Rogers MA; Radivojkov M; Tosti A; de Berker DA; Weinlich G; Schmuth M; Ruzicka T; Eckstein GN
Br J Dermatol; 2009 Mar; 160(3):527-33. PubMed ID: 19067701
[TBL] [Abstract][Full Text] [Related]
34. Genetic homogeneity, high-resolution mapping, and mutation analysis of the urofacial (Ochoa) syndrome and exclusion of the glutamate oxaloacetate transaminase gene (GOT1) in the critical region as the disease gene.
Wang CY; Huang YQ; Shi JD; Marron MP; Ruan QG; Hawkins-Lee B; Ochoa B; She JX
Am J Med Genet; 1999 Jun; 84(5):454-9. PubMed ID: 10360399
[TBL] [Abstract][Full Text] [Related]
35. A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2.
Lo Nigro C; Cusano R; Scaranari M; Cinti R; Forabosco P; Morra VB; De Michele G; Santoro L; Davies S; Hurst J; Devoto M; Ravazzolo R; Seri M
Eur J Hum Genet; 2000 Oct; 8(10):777-82. PubMed ID: 11039578
[TBL] [Abstract][Full Text] [Related]
36. A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.
Hameed A; Khaliq S; Ismail M; Anwar K; Mehdi SQ; Bessant D; Payne AM; Bhattacharya SS
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1436-8. PubMed ID: 11381043
[TBL] [Abstract][Full Text] [Related]
37. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
Tariq M; Chishti MS; Ali G; Ahmad W
Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
[TBL] [Abstract][Full Text] [Related]
38. Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.
Liu NP; Dew-Knight S; Jonasson F; Gilbert JR; Klintworth GK; Vance JM
Mol Vis; 2000 Jun; 6():95-100. PubMed ID: 10869098
[TBL] [Abstract][Full Text] [Related]
39. [Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus].
Gong YQ; Li JX; Liu QJ; Chen BX; Guo CH; Gao GM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):53-5. PubMed ID: 12579502
[TBL] [Abstract][Full Text] [Related]
40. Refined mapping of the Cohen syndrome gene by linkage disequilibrium.
Kolehmainen J; Norio R; Kivitie-Kallio S; Tahvanainen E; de la Chapelle A; Lehesjoki AE
Eur J Hum Genet; 1997; 5(4):206-13. PubMed ID: 9359041
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
