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Methods in Molecular Biology (Clifton, N.J.)|March 23, 2018
Identification of Chromothripsis in Biopsy Using SNP-Based MicroarrayVeronica Ortega, Christina Mendiola, Gopalrao V N Velagaleti
Clinical Dysmorphology|May 29, 2009
The phenotypic spectrum of trisomy 2: report of two new casesErcan Mihci, Gopalrao V N Velagaleti, Regina Ensenauer, et al.
Cancer Genetics and Cytogenetics|September 1, 2010
Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?Anna D Asleson, Vickie Morgan, Stephen Smith, et al.
Case Reports in Genetics|July 11, 2013
Fetoplacental discrepancy with normal karyotype in amniotic fluid and two different cell lines in placentaVeronica Ortega, Christina Mendiola, Eric Williamson, et al.
Fetal Diagnosis and Therapy|November 13, 2004
Sonographic, pathologic and karyotypic findings in a rare case of placenta fenestrataJessica M Linhart, Marjorie R Grafe, George R Saade, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal refluxNeena L Champaigne, Nicole A Laird, Jill K Northup, et al.
Indian Journal of Pediatrics|June 24, 2008
Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large familyGopalrao V N Velagaleti, Judy C Hawkins, Neli I Panova, et al.
Cancer Genetics and Cytogenetics|January 22, 2002
Translocation (15;17) and trisomy 21 in the microgranular variant of acute promyelocytic leukemiaDerrick W Spell, Gopalrao V N Velagaleti, Dennie V Jones, et al.
Cancer Genetics and Cytogenetics|February 28, 2003
Cytogenetic findings in a case of nodular fasciitis of subclavicular regionGopalrao V N Velagaleti, Jill K Tapper, Neli E Panova, et al.
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