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American Journal of Medical Genetics|February 1, 1991
SV40-transformed fragile (X) amniocytesE C Jenkins, S E Brooks, S L Stark-Houck, et al.The Journal of Biological Chemistry|June 5, 1998
Identification of a candidate human spectrin Src homology 3 domain-binding protein suggests a general mechanism of association of tyrosine kinases with the spectrin-based membrane skeletonD Ziemnicka-Kotula, J Xu, H Gu, et al.Journal of Cellular Biochemistry|August 1, 1995
Light and electron microscopic immunocytochemical localization of two major proteins in garlic bulbG Y Wen, A Mato, H M Wisniewski, et al.Upsala Journal of Medical Sciences. Supplement|January 1, 1987
Genetics and expression of the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.Clinical Genetics|August 16, 2003
Association of autism severity with a monoamine oxidase A functional polymorphismI L Cohen, X Liu, C Schutz, et al.American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.In Vitro Cellular & Developmental Biology. Animal|April 1, 1994
Characterization of a strain of cerebral endothelial cells derived from goat brain which retain their differentiated traits after long-term passageL Faso, R S Trowbridge, W Quan, et al.Clinical Genetics|September 11, 1992
Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH)A Jeziorowska, G E Houck, X L Yao, et al.Genetic Testing|January 6, 2001
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinosesN A Zhong, K E Wisniewski, W Ju, et al.Progress in Clinical and Biological Research|January 1, 1983
Compliance with chemotherapy: theoretical basis and intervention designJ L Richardson, C A Johnson, J Selser, et al.Pageof 16