158 related articles for article (PubMed ID: 1427869)
1. The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.
Lyonnet S; Pelet A; Royer G; Delrieu O; Serville F; le Marec B; Gruensteudel A; Pfeiffer RA; Briard ML; Dubay C
Genomics; 1992 Oct; 14(2):508-10. PubMed ID: 1427869
[TBL] [Abstract][Full Text] [Related]
2. Further localization of X-linked hydrocephalus in the chromosomal region Xq28.
Willems PJ; Vits L; Raeymaekers P; Beuten J; Coucke P; Holden JJ; Van Broeckhoven C; Warren ST; Sagi M; Robinson D
Am J Hum Genet; 1992 Aug; 51(2):307-15. PubMed ID: 1642232
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28.
Lehesjoki AE; Sankila EM; Miao J; Somer M; Salonen R; Rapola J; de la Chapelle A
J Med Genet; 1990 May; 27(5):288-91. PubMed ID: 1972196
[TBL] [Abstract][Full Text] [Related]
5. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.
Yates JR; Warner JP; Smith JA; Deymeer F; Azulay JP; Hausmanowa-Petrusewicz I; Zaremba J; Borkowska J; Affara NA; Ferguson-Smith MA
J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613
[TBL] [Abstract][Full Text] [Related]
6. X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci.
Thomas NS; Williams H; Cole G; Roberts K; Clarke A; Liechti-Gallati S; Braga S; Gerber A; Meier C; Moser H
J Med Genet; 1990 May; 27(5):284-7. PubMed ID: 2352256
[TBL] [Abstract][Full Text] [Related]
7. Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere.
Mulligan LM; Grover HJ; Blanchette VS; Giles AR; Lillicrap DP; Phillips A; Holden JJ; White BN
Am J Med Genet; 1987 Mar; 26(3):751-60. PubMed ID: 3105317
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.
Willems PJ; Dijkstra I; Van der Auwera BJ; Vits L; Coucke P; Raeymaekers P; Van Broeckhoven C; Consalez GG; Freeman SB; Warren ST
Genomics; 1990 Oct; 8(2):367-70. PubMed ID: 1979056
[TBL] [Abstract][Full Text] [Related]
11. Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.
Bolhuis PA; Hensels GW; Hulsebos TJ; Baas F; Barth PG
Am J Hum Genet; 1991 Mar; 48(3):481-5. PubMed ID: 1998334
[TBL] [Abstract][Full Text] [Related]
12. DNA linkage analysis of 26 families with fragile X syndrome.
Carpenter NJ
Am J Med Genet; 1991; 38(2-3):311-8. PubMed ID: 1673303
[TBL] [Abstract][Full Text] [Related]
13. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
Nordström AM; Penttinen M; von Koskull H
Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558
[TBL] [Abstract][Full Text] [Related]
14. X-linked centronuclear myopathy: mapping the gene to Xq28.
Liechti-Gallati S; Müller B; Grimm T; Kress W; Müller C; Boltshauser E; Moser H; Braga S
Neuromuscul Disord; 1991; 1(4):239-45. PubMed ID: 1822801
[TBL] [Abstract][Full Text] [Related]
15. The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28.
Janssen EA; Hensels GW; van Oost BA; Hamel BC; Kemp S; Baas F; Weber JW; Barth PG; Bolhuis PA
Neuromuscul Disord; 1994; 4(5-6):455-61. PubMed ID: 7881289
[TBL] [Abstract][Full Text] [Related]
16. Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.
Sefiani A; M'rad R; Simard L; Vincent A; Julier C; Holvoet-Vermaut L; Heuertz S; Dahl N; Stalder JF; Peter MO
Hum Genet; 1991 Jan; 86(3):297-9. PubMed ID: 1847690
[TBL] [Abstract][Full Text] [Related]
17. The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28.
Smahi A; Hyden-Granskog C; Peterlin B; Vabres P; Heuertz S; Fulchignoni-Lataud MC; Dahl N; Labrune P; Le Marec B; Piussan C
Hum Mol Genet; 1994 Feb; 3(2):273-8. PubMed ID: 8004094
[TBL] [Abstract][Full Text] [Related]
18. X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees.
Berrettini WH; Goldin LR; Gelernter J; Gejman PV; Gershon ES; Detera-Wadleigh S
Arch Gen Psychiatry; 1990 Apr; 47(4):366-73. PubMed ID: 2322087
[TBL] [Abstract][Full Text] [Related]
19. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.
Brown WT; Gross AC; Goonewardena P; Ferrando C; Dobkin C; Jenkins EC
Am J Med Genet; 1991; 38(2-3):343-6. PubMed ID: 1673308
[TBL] [Abstract][Full Text] [Related]
20. A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.
Vincent A; Kretz C; Oberlé I; Mandel JL
Hum Genet; 1989 Apr; 82(1):85-6. PubMed ID: 2565870
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
