Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay

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American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2589-2592

John Wiley & Sons Inc

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NB4S , a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma

By Roberts T.   Chernova O.   Cowell J.K.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1169-1178

Oxford University Press

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In vivo analysis of mammary and non-mammary tumorigenesis in MMTV-cyclin D1 transgenic mice deficient in p53

By Hosokawa Y.  

Transgenic Research, Vol. 10, Iss. 5, 2001-10 ,pp. : 471-478

Springer Publishing Company

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Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes

By Basit Sulman   Ali Ghazanfar   Wasif Naveed   Ansar Muhammad   Ahmad Wasim  

Human Genetics, Vol. 128, Iss. 2, 2010-08 ,pp. : 213-220

Springer Publishing Company

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Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping

By Strautnieks Sandra S.   Thompson Richard J.   Hanukoglu Aaron   Dillon Michael J.   Hanukoglu Israel   Kuhnle Ursula   Seckl Jonathan   Gardiner R. Mark   Chung Eddie  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 293-299

Oxford University Press

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