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Clinical Genetics|September 1, 1995
Clinical phenotype associated with terminal 2q37 deletionB Conrad, G Dewald, E Christensen, et al.The Journal of Pediatrics|February 1, 1976
Rocking waterbeds and auditory stimuli to enhance growth of preterm infants. Preliminary reportL I Kramer, M E PierpontAmerican Journal of Medical Genetics|October 16, 1996
Variation in severity of cardiac disease in Holt-Oram syndromeL J Sletten, M E PierpontAmerican Journal of Medical Genetics|May 22, 1995
Familial occurrence of patent ductus arteriosusL J Sletten, M E PierpontMinnesota Medicine|February 1, 1992
The child at risk for developing heart disease. 3A P Rocchini, M E PierpontAnnales De L'Institut Pasteur. Immunology|September 1, 1988
Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samplesG DewaldAmerican Journal of Medical Genetics|October 6, 1999
Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndromeD Satran, M E Pierpont, W B DobynsClinical Genetics|February 1, 1987
Pseudodeficiency of arylsulfatase A: a counseling dilemmaS Baldinger, M E Pierpont, D A WengerVox Sanguinis|January 1, 1979
Polymorphism of the second component of human complement (C2). Observation of the rare phenotype (C2 2 (= C2 B) and data on the localization of the C2 locus in the HLA regionG Dewald, C RittnerThe Journal of Pediatrics|June 1, 1984
Single central incisor in familial holoprosencephalyS A Berry, M E Pierpont, R J GorlinPageof 529