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Journal Abstract Search
223 related items for PubMed ID: 1362559
1. 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. PubMed ID: 1362559 [Abstract] [Full Text] [Related]
5. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D. J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352 [Abstract] [Full Text] [Related]
8. The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21). Saugier-Veber P, Abadie V, Moncla A, Mathieu M, Piussan C, Turleau C, Mattei JF, Munnich A, Lyonnet S. Am J Hum Genet; 1993 Jun; 52(6):1040-5. PubMed ID: 8503439 [Abstract] [Full Text] [Related]
11. A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity. Reardon W, Middleton-Price HR, Sandkuijl L, Phelps P, Bellman S, Luxon L, Pembrey ME, Malcolm S. Genomics; 1991 Dec; 11(4):885-94. PubMed ID: 1783396 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
18. 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. PubMed ID: 2900806 [Abstract] [Full Text] [Related]