106 related articles for article (PubMed ID: 8012397)
1. The gene for achondroplasia maps to the telomeric region of chromosome 4p.
Velinov M; Slaugenhaupt SA; Stoilov I; Scott CI; Gusella JF; Tsipouras P
Nat Genet; 1994 Mar; 6(3):314-7. PubMed ID: 8012397
[TBL] [Abstract][Full Text] [Related]
2. A gene for achondroplasia-hypochondroplasia maps to chromosome 4p.
Le Merrer M; Rousseau F; Legeai-Mallet L; Landais JC; Pelet A; Bonaventure J; Sanak M; Weissenbach J; Stoll C; Munnich A
Nat Genet; 1994 Mar; 6(3):318-21. PubMed ID: 8012398
[TBL] [Abstract][Full Text] [Related]
3. A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia.
Stoilov I; Kilpatrick MW; Tsipouras P
Am J Med Genet; 1995 Jan; 55(1):127-33. PubMed ID: 7702086
[TBL] [Abstract][Full Text] [Related]
4. Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p.
Francomano CA; Ortiz de Luna RI; Hefferon TW; Bellus GA; Turner CE; Taylor E; Meyers DA; Blanton SH; Murray JC; McIntosh I
Hum Mol Genet; 1994 May; 3(5):787-92. PubMed ID: 8081365
[TBL] [Abstract][Full Text] [Related]
5. [Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
Ezquieta Zubicaray B; Iguacel AO; Varela Junquera JM; Jariego Fente CM; González Gancedo P; Gracia Bouthelier R
Med Clin (Barc); 1999 Mar; 112(8):290-3. PubMed ID: 10207844
[TBL] [Abstract][Full Text] [Related]
6. The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.
Polymeropoulos MH; Ide SE; Wright M; Goodship J; Weissenbach J; Pyeritz RE; Da Silva EO; Ortiz De Luna RI; Francomano CA
Genomics; 1996 Jul; 35(1):1-5. PubMed ID: 8661097
[TBL] [Abstract][Full Text] [Related]
7. Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromes.
Krakow D; Salazar D; Wilcox WR; Rimoin DL; Cohn DH
Eur J Hum Genet; 2000 Aug; 8(8):645-8. PubMed ID: 10951528
[TBL] [Abstract][Full Text] [Related]
8. The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.
Heutink P; Zguricas J; van Oosterhout L; Breedveld GJ; Testers L; Sandkuijl LA; Snijders PJ; Weissenbach J; Lindhout D; Hovius SE
Nat Genet; 1994 Mar; 6(3):287-92. PubMed ID: 8012392
[TBL] [Abstract][Full Text] [Related]
9. Index, comprehensive microsatellite, and unified linkage maps of human chromosome 14 with cytogenetic tie points and a telomere microsatellite marker.
Pandit SD; Wang JC; Veile RA; Mishra SK; Warlick CA; Donis-Keller H
Genomics; 1995 Oct; 29(3):653-64. PubMed ID: 8575758
[TBL] [Abstract][Full Text] [Related]
10. Chromosome 4p16 and osteochondroplasias.
Urioste M; Martinez-Frias ML; Bermejo E; Villa A; Jimenez N; Romero D; Nieto C
Nat Genet; 1994 Apr; 6(4):334. PubMed ID: 8054971
[No Abstract] [Full Text] [Related]
11. 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]
12. Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19.
Briggs MD; Rasmussen IM; Weber JL; Yuen J; Reinker K; Garber AP; Rimoin DL; Cohn DH
Genomics; 1993 Dec; 18(3):656-60. PubMed ID: 8307576
[TBL] [Abstract][Full Text] [Related]
13. Characterization of a susceptibility locus for SLE, SLEB5, on chromosome 4p14-13.
Johansson CM; Kristjánsdottir H; Gröndal G; Steinsson K; Alarcón-Riquelme ME
Scand J Immunol; 2006 Sep; 64(3):308-13. PubMed ID: 16918700
[TBL] [Abstract][Full Text] [Related]
14. A locus for bipolar affective disorder on chromosome 4p.
Blackwood DH; He L; Morris SW; McLean A; Whitton C; Thomson M; Walker MT; Woodburn K; Sharp CM; Wright AF; Shibasaki Y; St Clair DM; Porteous DJ; Muir WJ
Nat Genet; 1996 Apr; 12(4):427-30. PubMed ID: 8630499
[TBL] [Abstract][Full Text] [Related]
15. A primary genetic linkage map of 14 polymorphic loci for the short arm of human chromosome 8.
Emi M; Fujiwara Y; Nakamura Y
Genomics; 1993 Mar; 15(3):530-4. PubMed ID: 8096828
[TBL] [Abstract][Full Text] [Related]
16. An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36.
Radhakrishna U; Blouin JL; Solanki JV; Dhoriani GM; Antonarakis SE
Am J Med Genet; 1996 Dec; 66(2):209-15. PubMed ID: 8958333
[TBL] [Abstract][Full Text] [Related]
17. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).
Oetting WS; Armstrong CM; Holleschau AM; DeWan AT; Summers GC
Ophthalmic Genet; 2000 Dec; 21(4):227-33. PubMed ID: 11135493
[TBL] [Abstract][Full Text] [Related]
18. Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease.
Peters DJ; Spruit L; Saris JJ; Ravine D; Sandkuijl LA; Fossdal R; Boersma J; van Eijk R; Nørby S; Constantinou-Deltas CD
Nat Genet; 1993 Dec; 5(4):359-62. PubMed ID: 8298643
[TBL] [Abstract][Full Text] [Related]
19. Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees.
Camp NJ; Farnham JM; Cannon-Albright LA
Cancer Res; 2006 Oct; 66(20):10205-12. PubMed ID: 17047086
[TBL] [Abstract][Full Text] [Related]
20. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.
Innis JW; Asher JH; Liang Y; Wang A; Wilke CM; Dierick HA; Kazen-Gillespie K; Sheldon S; Glover TW; Friedman TB
Am J Med Genet; 1997 Aug; 71(3):292-7. PubMed ID: 9268099
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]