120 related articles for article (PubMed ID: 8307576)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)].
Ikegawa S; Ohashi H; Hosoda F; Fukushima Y; Ohki M; Nakamura Y
Am J Med Genet; 1998 Jun; 77(5):356-9. PubMed ID: 9632164
[TBL] [Abstract][Full Text] [Related]
8. Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.
Johnson AT; Richards JE; Boehnke M; Stringham HM; Herman SB; Wong DJ; Lichter PR
Ophthalmology; 1996 May; 103(5):808-14. PubMed ID: 8637692
[TBL] [Abstract][Full Text] [Related]
9. A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.
Bamshad M; Watkins WS; Zenger RK; Bohnsack JF; Carey JC; Otterud B; Krakowiak PA; Robertson M; Jorde LB
Am J Hum Genet; 1994 Dec; 55(6):1153-8. PubMed ID: 7977374
[TBL] [Abstract][Full Text] [Related]
10. Linkage analysis of a large pedigree with hereditary sideroblastic anaemia.
Noble JS; Taylor GR; Losowsky MS; Hall R; Turner G; Mueller RF; Stewart AD
J Med Genet; 1995 May; 32(5):389-92. PubMed ID: 7616548
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Pseudoachondroplasia and multiple epiphyseal dysplasia: New etiologic developments.
Unger S; Hecht JT
Am J Med Genet; 2001; 106(4):244-50. PubMed ID: 11891674
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia.
Finkelstein JE; Doege K; Yamada Y; Pyeritz RE; Graham JM; Moeschler JB; Pauli RM; Hecht JT; Francomano CA
Am J Hum Genet; 1991 Jan; 48(1):97-102. PubMed ID: 1670752
[TBL] [Abstract][Full Text] [Related]
16. Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypes.
Slaugenhaupt SA; Acierno JS; Helbling LA; Bove C; Goldin E; Bach G; Schiffmann R; Gusella JF
Am J Hum Genet; 1999 Sep; 65(3):773-8. PubMed ID: 10441585
[TBL] [Abstract][Full Text] [Related]
17. The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17.
Pulst SM; Graham JM; Fain P; Barker D; Pribyl T; Korenberg JR
Hum Genet; 1990 Jun; 85(1):12-4. PubMed ID: 2162805
[TBL] [Abstract][Full Text] [Related]
18. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.
Korneluk RG; MacKenzie AE; Nakamura Y; Dubé I; Jacob P; Hunter AG
Genomics; 1989 Oct; 5(3):596-604. PubMed ID: 2613241
[TBL] [Abstract][Full Text] [Related]
19. Twenty loci form a continuous linkage map of markers for human chromosome 2.
O'Connell P; Lathrop GM; Nakamura Y; Leppert ML; Lalouel JM; White R
Genomics; 1989 Nov; 5(4):738-45. PubMed ID: 2591961
[TBL] [Abstract][Full Text] [Related]
20. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10.
Wu JS; Myers S; Carson N; Kidd JR; Anderson L; Castiglione CM; Hoyle LS; Lichter JB; Sukhatme VP; Simpson NE
Genomics; 1990 Nov; 8(3):461-8. PubMed ID: 1981049
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
