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3. Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome. Gedeon AK; Kozman HM; Robinson H; Pilia G; Schlessinger D; Turner G; Mulley JC Am J Med Genet; 1996 Jul; 64(1):63-8. PubMed ID: 8826450 [TBL] [Abstract][Full Text] [Related]
4. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus. Carpenter NJ; Thibodeau SN; Brown WT Am J Med Genet; 1991; 38(2-3):349-53. PubMed ID: 1673310 [TBL] [Abstract][Full Text] [Related]
5. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701 [TBL] [Abstract][Full Text] [Related]
6. Congenital motor nystagmus linked to Xq26-q27. Kerrison JB; Vagefi MR; Barmada MM; Maumenee IH Am J Hum Genet; 1999 Feb; 64(2):600-7. PubMed ID: 9973299 [TBL] [Abstract][Full Text] [Related]
7. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome. Thibodeau SN; Dorkins HR; Faulk KR; Berry R; Smith AC; Hagerman R; King A; Davies KE Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993 [TBL] [Abstract][Full Text] [Related]
8. mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation. Mumm S; Whyte MP; Thakker RV; Buetow KH; Schlessinger D Am J Hum Genet; 1997 Jan; 60(1):153-9. PubMed ID: 8981958 [TBL] [Abstract][Full Text] [Related]
9. Genetic mapping of new RFLPs at Xq27-q28. Suthers GK; Oberlé I; Nancarrow J; Mulley JC; Hyland VJ; Wilson PJ; McCure J; Morris CP; Hopwood JJ; Mandel JL Genomics; 1991 Jan; 9(1):37-43. PubMed ID: 1672291 [TBL] [Abstract][Full Text] [Related]
10. Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26. Yntema HG; Hamel BC; Smits AP; van Roosmalen T; van den Helm B; Kremer H; Ropers HH; Smeets DF; van Bokhoven H J Med Genet; 1998 Oct; 35(10):801-5. PubMed ID: 9783701 [TBL] [Abstract][Full Text] [Related]
11. Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27. Turner G; Gedeon A; Mulley J; Sutherland G; Rae J; Power K; Arthur I Am J Med Genet; 1989 Dec; 34(4):463-9. PubMed ID: 2624253 [TBL] [Abstract][Full Text] [Related]
12. Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus. Knoers N; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH Genomics; 1989 Apr; 4(3):434-7. PubMed ID: 2714800 [TBL] [Abstract][Full Text] [Related]
13. More precise localization of the gene for Hunter syndrome. Le Guern E; Couillin P; Oberlé I; Ravise N; Boue J Genomics; 1990 Jul; 7(3):358-62. PubMed ID: 2114352 [TBL] [Abstract][Full Text] [Related]
14. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation. Gedeon AK; Glass IA; Connor JM; Mulley JC Am J Med Genet; 1996 Jul; 64(1):121-4. PubMed ID: 8826461 [TBL] [Abstract][Full Text] [Related]
15. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions. Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932 [TBL] [Abstract][Full Text] [Related]
16. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA. Sauer SM; Phelan MC; Richer CL; Schwartz CE Cytogenet Cell Genet; 1989; 50(2-3):172-3. PubMed ID: 2776486 [TBL] [Abstract][Full Text] [Related]
17. Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Casey B; Devoto M; Jones KL; Ballabio A Nat Genet; 1993 Dec; 5(4):403-7. PubMed ID: 8298651 [TBL] [Abstract][Full Text] [Related]
18. Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3. Solomon NM; Ross SA; Morgan T; Belsky JL; Hol FA; Karnes PS; Hopwood NJ; Myers SE; Tan AS; Warne GL; Forrest SM; Thomas PQ J Med Genet; 2004 Sep; 41(9):669-78. PubMed ID: 15342697 [TBL] [Abstract][Full Text] [Related]
19. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan. Ansar M; Ramzan M; Pham TL; Yan K; Jamal SM; Haque S; Ahmad W; Leal SM Hum Hered; 2003; 55(1):71-4. PubMed ID: 12890929 [TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1). Kerrison JB; Giorda R; Lenart TD; Drack AV; Maumenee IH Ophthalmic Genet; 2001 Dec; 22(4):241-8. PubMed ID: 11803490 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]