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Clinical Genetics|June 1, 1987
Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) matJ T Martsolf, T R Chase, S M Jalal, et al.Mayo Clinic Proceedings|February 24, 1998
Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridizationS M Jalal, M E Law, R O Carlson, et al.Human Genetics|January 1, 1989
Familial transmission of 16p trisomy in an infantS M Jalal, D W Day, M Garcia, et al.Clinical Dysmorphology|August 5, 1998
Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughtersD Babovic-Vuksanovic, J A Westman, S M Jalal, et al.American Journal of Medical Genetics|December 1, 1990
Euchromatic 16p+ heteromorphism: first report in North AmericaS M Jalal, N R Schneider, M K Kukolich, et al.American Journal of Medical Genetics|February 2, 1996
Dynamics of chromosome spreadingJ L Spurbeck, A R Zinsmeister, K J Meyer, et al.Cancer Genetics and Cytogenetics|July 1, 1993
Frequency and photographs of HGM11 chromosome anomalies in bone marrow samples from 3,996 patients with malignant hematologic neoplasmsG W Dewald, C R Schad, V C Lilla, et al.American Journal of Medical Genetics|December 23, 1999
Ring chromosome 8 syndrome: further characterizationV S Tonk, M K Kukolich, D Morgan, et al.American Journal of Medical Genetics. Part A|January 7, 2004
Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardationDusica Babovic-Vuksanovic, S C Jenkins, R Ensenauer, et al.Clinical Genetics|January 1, 1991
Tetrasomy 9p: an emerging syndromeS M Jalal, M K Kukolich, M Garcia, et al.Pageof 8