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Journal of Sex & Marital Therapy|May 26, 2009
Exploring relationships of psychopathology in hypersexual patients using the MMPI-2Rory C Reid, Bruce N CarpenterThe Journal of the Oklahoma State Medical Association|March 21, 1998
Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosisB Can, F V Schaefer, S Malik, et al.Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.Bollettino Dell'Istituto Sieroterapico Milanese|July 31, 1978
Progress report on immunotherapy of chronic myeloid leukemiaJ E Sokal, N Carpenter, C NizetAmerican Journal of Medical Genetics|November 1, 1986
New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 3, 2001
Quantitative amino acid analysis using a Beckman system gold HPLC 126AA analyzerY Qu, R H Slocum, J Fu, et al.Journal of Neuroscience Research|September 11, 2001
Malonyl CoA decarboxylase deficiency: C to T transition in intron 2 of the MCD geneS Surendran, K A Sacksteder, S J Gould, et al.American Journal of Medical Genetics|July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridizationV V Rao, N J Carpenter, M Gucsavas, et al.Annales De Genetique|January 1, 1996
Familial deletion of chromosome 18 (p11.2)G V Velagaleti, S Harris, N J Carpenter, et al.Pageof 11