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Human Molecular Genetics|March 28, 2009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingClaudia M B Carvalho, Feng Zhang, Pengfei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2006
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridizationTrilochan Sahoo, Sau Wai Cheung, Patricia Ward, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
A therapeutic trial of pro-methylation dietary supplements in Angelman syndromeLynne M Bird, Wen-Hann Tan, Carlos A Bacino, et al.
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypesJill A Rosenfeld, Lindsey E Stephens, Justine Coppinger, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Angelman syndrome: Mutations influence features in early childhoodWen-Hann Tan, Carlos A Bacino, Steven A Skinner, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|December 21, 2019
Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypesYassemine Khawajkie, Nawel Mechtouf, Ngoc Minh Phuong Nguyen, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 14, 2020
Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypesYassemine Khawajkie, Nawel Mechtouf, Ngoc Minh Phuong Nguyen, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utilityJia-Chi Wang, Leslie Ross, Loretta W Mahon, et al.
Neurogenetics|January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
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