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26. Linkage analysis of two families with X-linked recessive congenital motor nystagmus. Guo X; Li S; Jia X; Xiao X; Wang P; Zhang Q J Hum Genet; 2006; 51(1):76-80. PubMed ID: 16240070 [TBL] [Abstract][Full Text] [Related]
27. Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. Williamson C; Cavaco BM; Jauch A; Dixon PH; Forbes S; Harding B; Holtgreve-Grez H; Schoell B; Pereira MC; Font AP; Loureiro MM; Sobrinho LG; Santos MA; Thakker RV J Bone Miner Res; 1999 Feb; 14(2):230-9. PubMed ID: 9933477 [TBL] [Abstract][Full Text] [Related]
28. Refining the genetic location of the gene for X linked hydrocephalus within Xq28. Jouet M; Feldman E; Yates J; Donnai D; Paterson J; Siggers D; Kenwrick S J Med Genet; 1993 Mar; 30(3):214-7. PubMed ID: 8474107 [TBL] [Abstract][Full Text] [Related]
29. Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present. Schwartz C; Fitch N; Phelan MC; Richer CL; Stevenson R Hum Genet; 1987 May; 76(1):54-7. PubMed ID: 3471705 [TBL] [Abstract][Full Text] [Related]
30. Exclusion of close linkage between the parathyroid hormone gene and a mutant gene locus causing idiopathic hypoparathyroidism. Schmidtke J; Kruse K; Pape B; Sippell G J Med Genet; 1986 Jun; 23(3):217-9. PubMed ID: 3014148 [TBL] [Abstract][Full Text] [Related]
31. Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred. Whyte MP; Weldon VV J Pediatr; 1981 Oct; 99(4):608-11. PubMed ID: 7196945 [No Abstract] [Full Text] [Related]
32. Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes. Hol FA; Schepens MT; van Beersum SE; Redolfi E; Affer M; Vezzoni P; Hamel BC; Karnes PS; Mariman EC; Zucchi I Genomics; 2000 Oct; 69(2):174-81. PubMed ID: 11031100 [TBL] [Abstract][Full Text] [Related]
33. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies. Scheinman SJ; Pook MA; Wooding C; Pang JT; Frymoyer PA; Thakker RV J Clin Invest; 1993 Jun; 91(6):2351-7. PubMed ID: 8099916 [TBL] [Abstract][Full Text] [Related]
35. Bridging markers defining the map position of X linked hypophosphataemic rickets. Thakker RV; Read AP; Davies KE; Whyte MP; Weksberg R; Glorieux F; Davies M; Mountford RC; Harris R; King A J Med Genet; 1987 Dec; 24(12):756-60. PubMed ID: 2828625 [TBL] [Abstract][Full Text] [Related]
36. Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. Siniscalco M; Oberlé I; Melis P; Alhadeff B; Murray J; Filippi G; Mattioni T; Chen YT; Furneaux H; Old LJ Am J Med Genet; 1991; 38(2-3):357-62. PubMed ID: 1708201 [TBL] [Abstract][Full Text] [Related]
37. X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase. Andrew Nesbit M; Bowl MR; Harding B; Schlessinger D; Whyte MP; Thakker RV Genomics; 2004 Dec; 84(6):1060-70. PubMed ID: 15533723 [TBL] [Abstract][Full Text] [Related]
39. Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis. Tantravahi U; Murty VV; Jhanwar SC; Toole JJ; Woozney JM; Chaganti RS; Latt SA Cytogenet Cell Genet; 1986; 42(1-2):75-9. PubMed ID: 3013509 [TBL] [Abstract][Full Text] [Related]
40. X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26. Lagerström-Fermér M; Sundvall M; Johnsen E; Warne GL; Forrest SM; Zajac JD; Rickards A; Ravine D; Landegren U; Pettersson U Am J Hum Genet; 1997 Apr; 60(4):910-6. PubMed ID: 9106538 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]