Showing results (141-150 of 215) with videos related to
Sort By:
Pageof 22
Journal of Medical Genetics|January 8, 2008
Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platformE Aston, H Whitby, T Maxwell, et al.American Journal of Medical Genetics|September 19, 1997
Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15S W Cheung, L G Shaffer, C S Richards, et al.Clinical Genetics|September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormalityH A Heilstedt, B C Ballif, L A Howard, et al.Human Molecular Genetics|September 1, 1996
Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formationS L Page, J C Shin, J Y Han, et al.Prenatal Diagnosis|November 1, 1995
Mosaicism for trisomy 12: four cases with varying outcomesF Z Bischoff, J Zenger-Hain, D Moses, et al.American Journal of Human Genetics|October 6, 2000
Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndromeY Q Wu, J L Badano, C McCaskill, et al.American Journal of Medical Genetics|December 14, 1999
De novo direct duplication of 15q15-->q24 in a newborn boy with mild manifestationsJ Y Han, K H Kim, H D Lee, et al.Cancer Genetics and Cytogenetics|December 6, 2001
Cytogenetic-clinicopathologic correlations in rhabdomyosarcoma: a report of five casesZ Chen, C M Coffin, L M Smith, et al.Journal of Medical Genetics|April 17, 2008
Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studiesS T South, A F Rope, A N Lamb, et al.American Journal of Medical Genetics|December 1, 1993
Prenatal diagnosis and clinical findings in a case of hexasomy 12pI B Van den Veyver, M E Macha, C McCaskill, et al.Pageof 22