120 related articles for article (PubMed ID: 8307577)
1. Linkage of typical pseudoachondroplasia to chromosome 19.
Hecht JT; Francomano CA; Briggs MD; Deere M; Conner B; Horton WA; Warman M; Cohn DH; Blanton SH
Genomics; 1993 Dec; 18(3):661-6. PubMed ID: 8307577
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene.
Briggs MD; Hoffman SM; King LM; Olsen AS; Mohrenweiser H; Leroy JG; Mortier GR; Rimoin DL; Lachman RS; Gaines ES
Nat Genet; 1995 Jul; 10(3):330-6. PubMed ID: 7670472
[TBL] [Abstract][Full Text] [Related]
4. High-resolution genetic and physical mapping of multiple epiphyseal dysplasia and pseudoachondroplasia mutations at chromosome 19p13.1-p12.
Knowlton RG; Cekleniak JA; Cohn DH; Briggs MD; Hoffman SM; Brandriff BF; Olsen AS
Genomics; 1995 Aug; 28(3):513-9. PubMed ID: 7490089
[TBL] [Abstract][Full Text] [Related]
5. Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19.
Oehlmann R; Summerville GP; Yeh G; Weaver EJ; Jimenez SA; Knowlton RG
Am J Hum Genet; 1994 Jan; 54(1):3-10. PubMed ID: 8279467
[TBL] [Abstract][Full Text] [Related]
6. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.
Ducros A; Nagy T; Alamowitch S; Nibbio A; Joutel A; Vahedi K; Chabriat H; Iba-Zizen MT; Julien J; Davous P; Goas JY; Lyon-Caen O; Dubois B; Ducrocq X; Salsa F; Ragno M; Burkhard P; Bassetti C; Hutchinson M; Vérin M; Viader F; Chapon F; Levasseur M; Mas JL; Delrieu O
Am J Hum Genet; 1996 Jan; 58(1):171-81. PubMed ID: 8554054
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.
Hecht JT; Nelson LD; Crowder E; Wang Y; Elder FF; Harrison WR; Francomano CA; Prange CK; Lennon GG; Deere M
Nat Genet; 1995 Jul; 10(3):325-9. PubMed ID: 7670471
[TBL] [Abstract][Full Text] [Related]
9. Mosaicism in pseudoachondroplasia.
Ferguson HL; Deere M; Evans R; Rotta J; Hall JG; Hecht JT
Am J Med Genet; 1997 Jun; 70(3):287-91. PubMed ID: 9188668
[TBL] [Abstract][Full Text] [Related]
10. Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.
Gertner JM; Whyte MP; Dixon PH; Pang JT; Trump D; Pearce SH; Wooding C; Thakker RV
J Bone Miner Res; 1997 Aug; 12(8):1204-9. PubMed ID: 9258750
[TBL] [Abstract][Full Text] [Related]
11. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A locus for autosomal dominant anterior polar cataract on chromosome 17p.
Berry V; Ionides AC; Moore AT; Plant C; Bhattacharya SS; Shiels A
Hum Mol Genet; 1996 Mar; 5(3):415-9. PubMed ID: 8852669
[TBL] [Abstract][Full Text] [Related]
14. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].
Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW
Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426
[TBL] [Abstract][Full Text] [Related]
15. Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene.
Briggs MD; Choi H; Warman ML; Loughlin JA; Wordsworth P; Sykes BC; Irven CM; Smith M; Wynne-Davies R; Lipson MH
Am J Hum Genet; 1994 Oct; 55(4):678-84. PubMed ID: 7942845
[TBL] [Abstract][Full Text] [Related]
16. A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.
Inglehearn CF; Carter SA; Keen TJ; Lindsey J; Stephenson AM; Bashir R; al-Maghtheh M; Moore AT; Jay M; Bird AC
Nat Genet; 1993 May; 4(1):51-3. PubMed ID: 8513323
[TBL] [Abstract][Full Text] [Related]
17. A progressive early onset cataract gene maps to human chromosome 17q24.
Armitage MM; Kivlin JD; Ferrell RE
Nat Genet; 1995 Jan; 9(1):37-40. PubMed ID: 7704021
[TBL] [Abstract][Full Text] [Related]
18. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
Blanton SH; Heckenlively JR; Cottingham AW; Friedman J; Sadler LA; Wagner M; Friedman LH; Daiger SP
Genomics; 1991 Dec; 11(4):857-69. PubMed ID: 1783394
[TBL] [Abstract][Full Text] [Related]
19. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.
Forsman K; Lind L; Bäckman B; Westermark E; Holmgren G
Hum Mol Genet; 1994 Sep; 3(9):1621-5. PubMed ID: 7833920
[TBL] [Abstract][Full Text] [Related]
20. An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.
Millán JM; Martínez F; Vilela C; Beneyto M; Prieto F; Nájera C
Hum Genet; 1995 Aug; 96(2):216-8. PubMed ID: 7635473
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
