Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome

By Kalatzis V.   Abdelhak S.   Compain S.   Vincent C.   Petit C.  

Genomics, Vol. 34, Iss. 3, 1996-05 ,pp. : 422-425

Academic Press

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Volume 34, Number 3 (1996), in the article "Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome," by Vasiliki Kalatzis, Sonia Abdelhak, Sylvie Compain, Christop

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Genomics, Vol. 38, Iss. 1, 1996-11 ,pp. : 108-108

Academic Press

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Two novel single nucleotide polymorphisms (SNPs) and 4-bp deletion mutation of RBP4 gene in Chinese cattle

By Wang Mou  

Journal of Genetics, Vol. 89, Iss. 2, 2010-08 ,pp. : 233-236

Springer Publishing Company

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Genomic Organization of the Faciogenital Dysplasia (FGD1; Aarskog Syndrome) Gene

By Pasteris N.G.   Buckler J.   Cadle A.B.   Gorski J.L.  

Genomics, Vol. 43, Iss. 3, 1997-08 ,pp. : 390-394

Academic Press

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Rearrangement of the Human CDC5L Gene by a t(6;19)(p21;q13.1) in a Patient with Multicystic Renal Dysplasia

By Groenen P.M.A.   vanderlinden G.   devriendt K.   Fryns J.P.   van de Ven W.J.M.  

Genomics, Vol. 49, Iss. 2, 1998-04 ,pp. : 218-229

Academic Press

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