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Results: 1 to 20 of 182

1.

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.

PMID:
2904407
[PubMed - indexed for MEDLINE]
2.

Multipoint linkage analysis in X-linked Alport syndrome.

Hertz JM, Kruse TA, Thomsen A, Spencer ES.

Hum Genet. 1991 Dec;88(2):157-61.

PMID:
1684562
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
3199669
[PubMed - indexed for MEDLINE]
4.

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Bleeker-Wagemakers LM, Friedrich U, Gal A, Wienker TF, Warburg M, Ropers HH.

Hum Genet. 1985;71(3):211-4.

PMID:
2998969
[PubMed - indexed for MEDLINE]
5.

Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.

Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.

Nephrol Dial Transplant. 1989;4(12):1016-21.

PMID:
2517321
[PubMed - indexed for MEDLINE]
6.

Apparently changing patterns of inheritance in Alport's hereditary nephritis: genetic heterogeneity versus altered diagnostic criteria.

Evans SH, Erickson RP, Kelsch R, Peirce JC.

Clin Genet. 1980 Apr;17(4):285-92.

PMID:
7371220
[PubMed - indexed for MEDLINE]
7.

Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.

Saviranta P, Lindlöf M, Lehesjoki AE, Kalimo H, Lang H, Sonninen V, Savontaus ML, de la Chapelle A.

Am J Hum Genet. 1988 Jan;42(1):84-8.

PMID:
2892402
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Mapping of Alport syndrome to the long arm of the X chromosome.

Atkin CL, Hasstedt SJ, Menlove L, Cannon L, Kirschner N, Schwartz C, Nguyen K, Skolnick M.

Am J Hum Genet. 1988 Feb;42(2):249-55.

PMID:
3422540
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Genetics of classic Alport's syndrome.

Flinter FA, Cameron JS, Chantler C, Houston I, Bobrow M.

Lancet. 1988 Oct 29;2(8618):1005-7. Review.

PMID:
2902439
[PubMed - indexed for MEDLINE]
10.

Three new kindreds affected with Alport's syndrome.

Barbera G, Costanzi S, Sturniolo A, Passalacqua S, Splendiani G, Sangiorgi M, Attanasio A, Capria A, Federico F.

Contrib Nephrol. 1990;80:143-6. No abstract available.

PMID:
2282814
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
1684566
[PubMed - indexed for MEDLINE]
12.

[Alport's syndrome: apropos of 2 families].

Grünfeld JP.

Nephrologie. 2000;21(6):295-8. French.

PMID:
11117109
[PubMed - indexed for MEDLINE]
13.

DNA linkage analysis of X-linked retinoschisis.

Dahl N, Goonewardena P, Chotai J, Anvret M, Pettersson U.

Hum Genet. 1988 Mar;78(3):228-32.

PMID:
2894345
[PubMed - indexed for MEDLINE]
14.

Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome.

Turco AE, Bresin E, Rossetti S, Peterlin B, Morandi R, Pignatti PF.

Am J Kidney Dis. 1997 Aug;30(2):174-9.

PMID:
9261027
[PubMed - indexed for MEDLINE]
15.

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.

Peacocke M, Siminovitch KA.

Proc Natl Acad Sci U S A. 1987 May;84(10):3430-3.

PMID:
3472214
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.

Robinson D, Lamont M, Curtis G, Shields DC, Phelps P.

Hum Genet. 1992 Nov;90(3):316-8.

PMID:
1362559
[PubMed - indexed for MEDLINE]
17.

Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome.

Goonewardena P, Sjöholm AG, Nilsson LA, Pettersson U.

Genomics. 1988 Feb;2(2):115-8.

PMID:
2900806
[PubMed - indexed for MEDLINE]
18.

Alport's syndrome: genetic evaluation of personal data concerning twelve families.

Serbelloni P, Conte F, Gualandri V, Zanini M, Brambilla G, Pintucci JP, Sessa A.

Contrib Nephrol. 1990;80:126-30. No abstract available.

PMID:
2282810
[PubMed - indexed for MEDLINE]
19.

Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

MacDonald IM, Sandre RM, Wong P, Hunter AG, Tenniswood MP.

Hum Genet. 1987 Nov;77(3):233-5.

PMID:
2890569
[PubMed - indexed for MEDLINE]
20.

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, et al.

Hum Genet. 1987 Oct;77(2):172-4.

PMID:
2888720
[PubMed - indexed for MEDLINE]

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