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American Journal of Medical Genetics|December 1, 1987
Duplication of proximal 15q as a cause of Prader-Willi syndromeA L Pettigrew, S M Gollin, F Greenberg, et al.Human Genetics|January 1, 1984
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22F Greenberg, W E Crowder, V Paschall, et al.American Journal of Medical Genetics|April 1, 1986
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17F Greenberg, R F Stratton, L H Lockhart, et al.The Journal of Pediatrics|April 1, 1983
Miller-Dieker syndrome: lissencephaly and monosomy 17pW B Dobyns, R F Stratton, J T Parke, et al.Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.American Journal of Medical Genetics|January 1, 1987
The Gardner-Silengo-Wachtel or genito-palato-cardiac syndrome: male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal cardiac defectF Greenberg, M V Gresik, R J Carpenter, et al.American Journal of Medical Genetics|May 8, 1995
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter)A Scheuerle, J L Zenger-Hain, D L Van Dyke, et al.American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.Human Molecular Genetics|January 1, 1995
Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosisD H Ledbetter, E EngelHuman Genetics|August 24, 1999
Molecular cloning and characterization of the human NUDC geneN Matsumoto, D H LedbetterPageof 33