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Clinical Genetics|September 14, 2007
Non-random maternal X-chromosome inactivation associated with PHACESJ H Levin, S G KalerPediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 1999
Metabolic and molecular bases of Menkes disease and occipital horn syndromeS G KalerThe American Journal of Clinical Nutrition|May 20, 1998
Diagnosis and therapy of Menkes syndrome, a genetic form of copper deficiencyS G KalerBiological Trace Element Research|July 1, 1993
Application of a copper blotting method to the study of Menkes diseaseS G Kaler, W A GahlJournal of Craniofacial Genetics and Developmental Biology|January 1, 1982
Radiographic hand abnormalities in fifteen cases of Crouzon syndromeS G Kaler, D Bixler, P L YuBiochemical Medicine and Metabolic Biology|December 1, 1991
Human manganese superoxide dismutase is readily detectable by a copper blotting techniqueS G Kaler, R J Maraia, W A GahlAmerican Journal of Physical Anthropology|June 1, 1986
Metacarpophalangeal pattern profile analysis in clinical genetics: an applied anthropometric methodM G Butler, F J Meaney, S G KalerElectroencephalography and Clinical Neurophysiology|July 1, 1993
Spectrum of EEG findings in Menkes diseaseS R White, K Reese, S Sato, et al.Journal of Neurochemistry|November 1, 1996
Catecholamine phenotyping: clues to the diagnosis, treatment, and pathophysiology of neurogenetic disordersD S Goldstein, J W Lenders, S G Kaler, et al.Clinical Genetics|December 1, 1982
Metacarpophalangeal pattern profile analysis in Prader-Willi syndromeM G Butler, S G Kaler, P L Yu, et al.Pageof 4