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Items: 1 to 20 of 208

1.

A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.

Kibar Z, Lafrenière RG, Chakravarti A, Wang JC, Chevrette M, Der Kaloustian VM, Rouleau GA.

Genomics. 1999 Feb 15;56(1):127-30.

PMID:
10036193
2.

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q.

Kibar Z, Der Kaloustian VM, Brais B, Hani V, Fraser FC, Rouleau GA.

Hum Mol Genet. 1996 Apr;5(4):543-7.

3.

A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.

Lamartine J, Pitaval A, Soularue P, Lanneluc I, Lemaître G, Kibar Z, Rouleau GA, Waksman G.

Genomics. 2000 Jul 15;67(2):232-6.

PMID:
10903849
4.

The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.

Radhakrishna U, Blouin JL, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE.

Am J Med Genet. 1997 Jul 11;71(1):80-6.

PMID:
9215774
5.

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.

Kibar Z, Dubé MP, Powell J, McCuaïg C, Hayflick SJ, Zonana J, Hovnanian A, Radhakrishna U, Antonarakis SE, Benohanian A, Sheeran AD, Stephan ML, Gosselin R, Kelsell DP, Christianson AL, Fraser FC, Der Kaloustian VM, Rouleau GA.

Eur J Hum Genet. 2000 May;8(5):372-80.

6.

A radiation hybrid map of 95 STSs spanning human chromosome 13q.

Shaw SH, Farr JE, Thiel BA, Matise TC, Weissenbach J, Chakaravarti A, Richard CW 3rd.

Genomics. 1995 Jun 10;27(3):502-10.

PMID:
7558033
7.

Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family.

Lamartine J, Laoudj D, Blanchet-Bardon C, Kibar Z, Soularue P, Ridoux V, Dubertret L, Rouleau GA, Waksman G.

Br J Dermatol. 2000 Feb;142(2):248-52.

PMID:
10730756
8.

Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.

Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW, Heyberger S, Oudet C, Hanauer A.

Genomics. 1994 Aug;22(3):617-25.

PMID:
8001973
9.

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, et al.

Genomics. 1994 Sep 1;23(1):100-13.

10.

A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.

McPherson JD, Apostol B, Wagner-McPherson CB, Hakim S, Del Mastro RG, Aziz N, Baer E, Gonzales G, Krane MC, Markovich R, Masny P, Ortega M, Vu J, Vujicic M, Church DM, Segal A, Grady DL, Moyzis RK, Spence MA, Lovett M, Wasmuth JJ.

Genome Res. 1997 Sep;7(9):897-909.

11.

A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.

Tariq M, Chishti MS, Ali G, Ahmad W.

Ann Hum Genet. 2008 Jan;72(Pt 1):19-25. doi: 10.1111/j.1469-1809.2007.00391.x.

12.

A radiation hybrid map of human chromosome 18.

Francke U, Chang E, Comeau K, Geigl EM, Giacalone J, Li X, Luna J, Moon A, Welch S, Wilgenbus P.

Cytogenet Cell Genet. 1994;66(3):196-213.

PMID:
8125019
13.

Construction of a high-resolution RH map of the human 2q35 region on TNG panel and comparison with a physical map of the porcine homologous region 15q25.

Robic A, Jeon JT, Rey V, Amarger V, Chardon P, Looft C, Andersson L, Gellin J, Milan D.

Mamm Genome. 2001 May;12(5):380-6.

PMID:
11331947
15.

A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps.

Bihoreau MT, Sebag-Montefiore L, Godfrey RF, Wallis RH, Brown JH, Danoy PA, Collins SC, Rouard M, Kaisaki PJ, Lathrop M, Gauguier D.

Genomics. 2001 Jul;75(1-3):57-69.

PMID:
11472068
16.
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18.

A radiation hybrid map of the BRCA1 region of chromosome 17q12-q21.

Abel KJ, Boehnke M, Prahalad M, Ho P, Flejter WL, Watkins M, VanderStoep J, Chandrasekharappa SC, Collins FS, Glover TW, et al.

Genomics. 1993 Sep;17(3):632-41.

19.

A high resolution radiation hybrid map of bovine chromosome 14 identifies scaffold rearrangement in the latest bovine assembly.

Marques E, de Givry S, Stothard P, Murdoch B, Wang Z, Womack J, Moore SS.

BMC Genomics. 2007 Jul 26;8:254.

20.

A genetic linkage map of 96 loci on the short arm of human chromosome 3.

Tory K, Latif F, Modi W, Schmidt L, Wei MH, Li H, Cobler P, Orcutt ML, Delisio J, Geil L, et al.

Genomics. 1992 Jun;13(2):275-86.

PMID:
1612588
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