84 related articles for article (PubMed ID: 16525030)
1. Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14.
Warner JV; Nyholt DR; Busfield F; Epstein M; Burgess J; Stranks S; Hill P; Perry-Keene D; Learoyd D; Robinson B; Teh BT; Prins JB; Cardinal JW
J Med Genet; 2006 Mar; 43(3):e12. PubMed ID: 16525030
[TBL] [Abstract][Full Text] [Related]
2. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.
Teh BT; Farnebo F; Twigg S; Höög A; Kytölä S; Korpi-Hyövälti E; Wong FK; Nordenström J; Grimelius L; Sandelin K; Robinson B; Farnebo LO; Larsson C
J Clin Endocrinol Metab; 1998 Jun; 83(6):2114-20. PubMed ID: 9626148
[TBL] [Abstract][Full Text] [Related]
3. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
4. Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.
Wassif WS; Farnebo F; Teh BT; Moniz CF; Li FY; Harrison JD; Peters TJ; Larsson C; Harris P
Clin Endocrinol (Oxf); 1999 Feb; 50(2):191-6. PubMed ID: 10396361
[TBL] [Abstract][Full Text] [Related]
5. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
[TBL] [Abstract][Full Text] [Related]
6. The association of primary hyperparathyroidism and primary ovarian failure: a de novo t(X; 2) (q22p13) reciprocal translocation.
Bano G; Mansour S; Nussey S
Eur J Endocrinol; 2008 Feb; 158(2):261-3. PubMed ID: 18230835
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
Pankratz N; Nichols WC; Uniacke SK; Halter C; Murrell J; Rudolph A; Shults CW; Conneally PM; Foroud T;
Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570
[TBL] [Abstract][Full Text] [Related]
8. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH
J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119
[TBL] [Abstract][Full Text] [Related]
9. Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.
Mizusawa N; Uchino S; Iwata T; Tsuyuguchi M; Suzuki Y; Mizukoshi T; Yamashita Y; Sakurai A; Suzuki S; Beniko M; Tahara H; Fujisawa M; Kamata N; Fujisawa K; Yashiro T; Nagao D; Golam HM; Sano T; Noguchi S; Yoshimoto K
Clin Endocrinol (Oxf); 2006 Jul; 65(1):9-16. PubMed ID: 16817812
[TBL] [Abstract][Full Text] [Related]
10. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
Pang CP; Fan BJ; Canlas O; Wang DY; Dubois S; Tam PO; Lam DS; Raymond V; Ritch R
Mol Vis; 2006 Feb; 12():85-92. PubMed ID: 16518310
[TBL] [Abstract][Full Text] [Related]
11. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
[TBL] [Abstract][Full Text] [Related]
12. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
Jiao X; Ritter R; Hejtmancik JF; Edwards AO
Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4498-503. PubMed ID: 15557460
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3.
Van Vlijmen-Van Keulen CJ; Rauwerda JA; Pals G
Eur J Vasc Endovasc Surg; 2005 Jul; 30(1):29-35. PubMed ID: 15933979
[TBL] [Abstract][Full Text] [Related]
15. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
Lucas GJ; Riches PL; Hocking LJ; Cundy T; Nicholson GC; Walsh JP; Ralston SH
J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
[TBL] [Abstract][Full Text] [Related]
16. Refinement of 2q and 7p loci in a large multiplex NTD family.
Stamm DS; Siegel DG; Mehltretter L; Connelly JJ; Trott A; Ellis N; Zismann V; Stephan DA; George TM; Vekemans M; Ashley-Koch A; Gilbert JR; Gregory SG; Speer MC;
Birth Defects Res A Clin Mol Teratol; 2008 Jun; 82(6):441-52. PubMed ID: 18452155
[TBL] [Abstract][Full Text] [Related]
17. Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer.
Wassif WS; Moniz CF; Friedman E; Wong S; Weber G; Nordenskjöld M; Peters TJ; Larsson C
J Clin Endocrinol Metab; 1993 Dec; 77(6):1485-9. PubMed ID: 7903311
[TBL] [Abstract][Full Text] [Related]
18. Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.
Pras E; Aksentijevich I; Gruberg L; Balow JE; Prosen L; Dean M; Steinberg AD; Pras M; Kastner DL
N Engl J Med; 1992 Jun; 326(23):1509-13. PubMed ID: 1579134
[TBL] [Abstract][Full Text] [Related]
19. Surveillance for early detection of aggressive parathyroid disease: carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation.
Kelly TG; Shattuck TM; Reyes-Mugica M; Stewart AF; Simonds WF; Udelsman R; Arnold A; Carpenter TO
J Bone Miner Res; 2006 Oct; 21(10):1666-71. PubMed ID: 16995822
[TBL] [Abstract][Full Text] [Related]
20. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
