82 related articles for article (PubMed ID: 8954806)
21. Hereditary pancreatitis in a family of Aboriginal descent.
McGaughran JM; Kimble R; Upton J; George P
J Paediatr Child Health; 2004 Aug; 40(8):487-9. PubMed ID: 15265195
[TBL] [Abstract][Full Text] [Related]
22. Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.
Gao Q; Horwitz M; Roulston D; Hagos F; Zhao N; Freireich EJ; Golomb HM; Olopade OI
Genes Chromosomes Cancer; 2000 Jun; 28(2):164-72. PubMed ID: 10825001
[TBL] [Abstract][Full Text] [Related]
23. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF
Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487
[TBL] [Abstract][Full Text] [Related]
24. The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis.
Hedera P; Petty EM; Bui MR; Blaivas M; Fink JK
Arch Neurol; 2003 Sep; 60(9):1321-5. PubMed ID: 12975303
[TBL] [Abstract][Full Text] [Related]
25. Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family.
Kamatani N; Moritani M; Yamanaka H; Takeuchi F; Hosoya T; Itakura M
Arthritis Rheum; 2000 Apr; 43(4):925-9. PubMed ID: 10765940
[TBL] [Abstract][Full Text] [Related]
26. Implications of molecular diagnostic testing in families with hereditary pancreatitis.
Pandya A; Xia XJ; Blanton SH; Landa B; Markello T; Nance WE
Genet Test; 1997-1998; 1(3):207-11. PubMed ID: 10464647
[TBL] [Abstract][Full Text] [Related]
27. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
Levi A; Kohn Y; Kanyas K; Amann D; Pae CU; Hamdan A; Segman RH; Avidan N; Karni O; Korner M; Jun TY; Beckmann JS; Macciardi F; Lerer B
Eur J Hum Genet; 2005 Jun; 13(6):763-71. PubMed ID: 15812564
[TBL] [Abstract][Full Text] [Related]
28. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.
Mangino M; Flex E; Capon F; Sangiuolo F; Carraro E; Gualandi F; Mazzoli M; Martini A; Novelli G; Dallapiccola B
Eur J Hum Genet; 2001 Sep; 9(9):667-71. PubMed ID: 11571554
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
Kennerson M; Nicholson G; Kowalski B; Krajewski K; El-Khechen D; Feely S; Chu S; Shy M; Garbern J
Neurology; 2009 Jan; 72(3):246-52. PubMed ID: 19153371
[TBL] [Abstract][Full Text] [Related]
31. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
Plasilova M; Russell AM; Wanner A; Wolf A; Dobbie Z; Müller HJ; Heinimann K
Eur J Hum Genet; 2004 May; 12(5):365-71. PubMed ID: 14735163
[TBL] [Abstract][Full Text] [Related]
32. The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q.
Coucke P; Van Camp G; Demirhan O; Kabakkaya Y; Balemans W; Van Hauwe P; Van Agtmael T; Smith RJ; Parving A; Bolder CH; Cremers CW; Willems PJ
Genomics; 1997 Feb; 40(1):48-54. PubMed ID: 9070918
[TBL] [Abstract][Full Text] [Related]
33. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.
Notelet L; Chapon F; Khoury S; Vahedi K; Chodkiewicz JP; Courtheoux P; Iba-Zizen MT; Cabanis EA; Lechevalier B; Tournier-Lasserve E; Houtteville JP
J Neurol Neurosurg Psychiatry; 1997 Jul; 63(1):40-5. PubMed ID: 9221966
[TBL] [Abstract][Full Text] [Related]
34. Screening a family for hereditary chronic pancreatitis.
Nordback I; Saarenpää-Heikkilä O; Koskimies S
Panminerva Med; 1990; 32(1):19-24. PubMed ID: 2263397
[TBL] [Abstract][Full Text] [Related]
35. Hereditary pancreatitis: report of an affected Canadian kindred and review of the disease.
Girard RM; Dubé S; Archambault AP
Can Med Assoc J; 1981 Sep; 125(6):576-80. PubMed ID: 7026015
[TBL] [Abstract][Full Text] [Related]
36. [Chronic hereditary pancreatitis].
Ramos Lora M; Garrido Mora M; García Martín M; Ríos Ferrer T; Domínguez Macías A; Pujol de la Llave E; Rodríguez Rodríguez A
Rev Esp Enferm Dig; 1994 Aug; 86(2):622-4. PubMed ID: 7946611
[TBL] [Abstract][Full Text] [Related]
37. It takes a family.
Nat Genet; 1996 Oct; 14(2):117-8. PubMed ID: 8841172
[No Abstract] [Full Text] [Related]
38. Hereditary pancreatitis. Historical perspectives.
Perrault J
Med Clin North Am; 2000 May; 84(3):519-29, vii. PubMed ID: 10872411
[TBL] [Abstract][Full Text] [Related]
39. [Hereditary pancreatitis].
Klujber V; Klujber L
Orv Hetil; 1989 Aug; 130(33):1777-8. PubMed ID: 2505211
[TBL] [Abstract][Full Text] [Related]
40. Hereditary pancreatitis: early ultrasound appearances.
Spencer JA; Lindsell DR; Isaacs D
Pediatr Radiol; 1990; 20(4):293-5. PubMed ID: 2186349
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
