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Journal of Clinical Pathology|February 1, 1987
New marker of B lymphocytes, MB2: comparison with other lymphocyte subset markers active in conventionally processed tissue sectionsP A Hall, A J D'Ardenne, M G Butler, et al.Mental Retardation and Developmental Disabilities Research Reviews|July 19, 2000
Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndromeA Dimitropoulos, I D Feurer, E Roof, et al.Journal of Gerontology|March 1, 1983
A longitudinal study of nutritional intake in menV K Elahi, D Elahi, R Andres, et al.Human Molecular Genetics|April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patientY Sun, R D Nicholls, M G Butler, et al.Journal of Medical Genetics|March 19, 2002
Omphalocele in three generations with autosomal dominant transmissionS L Kanagawa, M L Begleiter, D J Ostlie, et al.American Journal of Human Genetics|August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5J Overhauser, U Bengtsson, J McMahon, et al.American Journal of Medical Genetics|January 1, 1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor geneE W Roback, A J Barakat, V G Dev, et al.American Journal of Medical Genetics|December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosisM G Butler, V G Dev, D Shah, et al.The British Journal of Ophthalmology|August 1, 1992
Fibronectin synthesis in subretinal membranes of proliferative vitreoretinopathyP Hiscott, H A Waller, I Grierson, et al.American Journal of Medical Genetics|May 8, 2000
Metacarpophalangeal pattern profile analysis in Noonan syndromeM G Butler, R Kumar, M F Davis, et al.Pageof 18