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Items: 5

1.

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Trump D, Dixon PH, Mumm S, Wooding C, Davies KE, Schlessinger D, Whyte MP, Thakker RV.

J Med Genet. 1998 Nov;35(11):905-9.

2.

Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectants.

Porteous DJ, Morten JE, Cranston G, Fletcher JM, Mitchell A, van Heyningen V, Fantes JA, Boyd PA, Hastie ND.

Mol Cell Biol. 1986 Jun;6(6):2223-32.

3.
4.

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.

van Heyningen V, Boyd PA, Seawright A, Fletcher JM, Fantes JA, Buckton KE, Spowart G, Porteous DJ, Hill RE, Newton MS, et al.

Proc Natl Acad Sci U S A. 1985 Dec;82(24):8592-6.

5.

DraII and XmnI polymorphisms at the human parathyroid hormone locus.

Shields JJ, Mullersman JE, Saha BK.

Nucleic Acids Res. 1991 Aug 11;19(15):4312. No abstract available.

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