Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2008
Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectivesSandra Darilek, Patricia Ward, Amber Pursley, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently "balanced" paracentric inversion of 14(q21q23)Yong-Hui Jiang, Jose E Martinez, Zhishuo Ou, et al.
Molecular Genetics and Metabolism|October 10, 2009
Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletionShulin Zhang, Fang-Yuan Li, Harold N Bass, et al.
Human Genetics|May 16, 2007
Male-to-female sex reversal associated with an approximately 250 kb deletion upstream of NR0B1 (DAX1)Marta Smyk, Jonathan S Berg, Amber Pursley, et al.
Prenatal Diagnosis|September 13, 2007
Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocationMarcia J Simovich, Svetlana A Yatsenko, Sung-Hae L Kang, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive casesJustin Pham, Chad Shaw, Amber Pursley, et al.
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.
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.
Journal of Medical Genetics|November 17, 2009
Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head sizeMarwan Shinawi, Pengfei Liu, Sung-Hae L Kang, et al.
Nature Genetics|November 26, 2008
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesNicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, et al.
Pageof 1