142 related articles for article (PubMed ID: 1684562)
1. Multipoint linkage analysis in X-linked Alport syndrome.
Hertz JM; Kruse TA; Thomsen A; Spencer ES
Hum Genet; 1991 Dec; 88(2):157-61. PubMed ID: 1684562
[TBL] [Abstract][Full Text] [Related]
2. Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88.
MacDermot KD; Morgan SH; Cheshire JK; Wilson TM
Hum Genet; 1987 Nov; 77(3):263-6. PubMed ID: 2890570
[TBL] [Abstract][Full Text] [Related]
3. Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.
Bergen AA; Samanns C; Schuurman EJ; van Osch L; van Dorp DB; Pinckers AJ; Bakker E; Gal A; van Ommen GJ; Bleeker-Wagemakers EM
Hum Genet; 1991 Dec; 88(2):162-6. PubMed ID: 1684563
[TBL] [Abstract][Full Text] [Related]
4. Linkage studies in X-linked Alport's syndrome.
Szpiro-Tapia S; Bobrie G; Guilloud-Bataille M; Heuertz S; Julier C; Frézal J; Grünfeld JP; Hors-Cayla MC
Hum Genet; 1988 Dec; 81(1):85-7. PubMed ID: 2904407
[TBL] [Abstract][Full Text] [Related]
5. X-linked megalocornea: close linkage to DXS87 and DXS94.
Chen JD; Mackey D; Fuller H; Serravalle S; Olsson J; Denton MJ
Hum Genet; 1989 Oct; 83(3):292-4. PubMed ID: 2571565
[TBL] [Abstract][Full Text] [Related]
6. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.
Kwan SP; Terwilliger J; Parmley R; Raghu G; Sandkuyl LA; Ott J; Ochs H; Wedgwood R; Rosen F
Genomics; 1990 Feb; 6(2):238-42. PubMed ID: 2307467
[TBL] [Abstract][Full Text] [Related]
7. Localization of the gene for classic Alport syndrome.
Flinter FA; Abbs S; Bobrow M
Genomics; 1989 Apr; 4(3):335-8. PubMed ID: 2565879
[TBL] [Abstract][Full Text] [Related]
8. Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).
Malcolm S; de Saint Basile G; Arveiler B; Lau YL; Szabo P; Fischer A; Griscelli C; Debre M; Mandel JL; Callard RE
Hum Genet; 1987 Oct; 77(2):172-4. PubMed ID: 2888720
[TBL] [Abstract][Full Text] [Related]
9. High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.
Barker DF; Fain PR; Goldgar DE; Dietz-Band JN; Turco AE; Kashtan CE; Gregory MC; Tryggvason K; Skolnick MH; Atkin CL
Hum Genet; 1991 Dec; 88(2):189-94. PubMed ID: 1684566
[TBL] [Abstract][Full Text] [Related]
10. Multipoint linkage analysis in Menkes disease.
Tønnesen T; Petterson A; Kruse TA; Gerdes AM; Horn N
Am J Hum Genet; 1992 May; 50(5):1012-7. PubMed ID: 1570830
[TBL] [Abstract][Full Text] [Related]
11. Choroideremia: linkage analysis with physically mapped close DNA-markers.
Sankila EM; Sistonen P; Cremers F; de la Chapelle A
Hum Genet; 1991 Jul; 87(3):348-52. PubMed ID: 1677924
[TBL] [Abstract][Full Text] [Related]
12. Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment.
Wieacker P; Griffin JE; Wienker T; Lopez JM; Wilson JD; Breckwoldt M
Hum Genet; 1987 Jul; 76(3):248-52. PubMed ID: 2885254
[TBL] [Abstract][Full Text] [Related]
13. Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.
Boespflug-Tanguy O; Mimault C; Melki J; Cavagna A; Giraud G; Pham Dinh D; Dastugue B; Dautigny A
Am J Hum Genet; 1994 Sep; 55(3):461-7. PubMed ID: 7915877
[TBL] [Abstract][Full Text] [Related]
14. Localization of the gene for X-linked Alport's syndrome.
Brunner H; Schröder C; van Bennekom C; Lambermon E; Tuerlings J; Menzel D; Olbing H; Monnens L; Wieringa B; Ropers HH
Kidney Int; 1988 Oct; 34(4):507-10. PubMed ID: 3199669
[TBL] [Abstract][Full Text] [Related]
15. Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.
Guioli S; Arveiler B; Bardoni B; Notarangelo LD; Panina P; Duse M; Ugazio A; Oberlé I; de Saint Basile G; Mandel JL
Hum Genet; 1989 Dec; 84(1):19-21. PubMed ID: 2575070
[TBL] [Abstract][Full Text] [Related]
16. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
Lesko JG; Lewis RA; Nussbaum RL
Am J Hum Genet; 1987 Apr; 40(4):303-11. PubMed ID: 2883887
[TBL] [Abstract][Full Text] [Related]
17. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
Schwartz CE; Ulmer J; Brown A; Pancoast I; Goodman HO; Stevenson RE
Am J Hum Genet; 1990 Sep; 47(3):454-8. PubMed ID: 2393020
[TBL] [Abstract][Full Text] [Related]
18. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
Arveiler B; Oberlé I; Mandel JL
Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
[TBL] [Abstract][Full Text] [Related]
19. Alport syndrome: a genetic study of 31 families.
M'Rad R; Sanak M; Deschenes G; Zhou J; Bonaiti-Pellie C; Holvoet-Vermaut L; Heuertz S; Gubler MC; Broyer M; Grunfeld JP
Hum Genet; 1992 Dec; 90(4):420-6. PubMed ID: 1483700
[TBL] [Abstract][Full Text] [Related]
20. Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
Biancalana V; Briard ML; David A; Gilgenkrantz S; Kaplan J; Mathieu M; Piussan C; Poncin J; Schinzel A; Oudet C
Am J Hum Genet; 1992 May; 50(5):981-7. PubMed ID: 1349200
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]