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American Journal of Medical Genetics|March 3, 1997
New syndrome of spondylospinal thoracic dysostosis with multiple pterygia and arthrogryposisV P Johnson, L D Keppen, M S Carpenter, et al.American Journal of Medical Genetics|March 3, 1997
Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelaeB Rouse, C Azen, R Koch, et al.American Journal of Medical Genetics|December 18, 1996
Angelman syndrome in adulthoodL A Laan, A T den Boer, R C Hennekam, et al.American Journal of Medical Genetics|March 31, 1997
Association of prenatal vascular disruptions with decreased maternal ageM S LubinskyAmerican Journal of Medical Genetics|March 31, 1997
Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?H Kawame, R A Pagon, L HudginsAmerican Journal of Medical Genetics|March 31, 1997
Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delayM Feingold, B D Hall, Y Lacassie, et al.American Journal of Medical Genetics|March 31, 1997
Multiple endocrinopathies in an infant with fatal neurodegenerative diseaseR R Shankar, A Haider, W T Garvey, et al.American Journal of Medical Genetics|March 31, 1997
Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interactionJ F Korczak, J S Brahim, J J DiGiovanna, et al.American Journal of Medical Genetics|March 31, 1997
Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratoryL G Shaffer, G M Kennedy, A S Spikes, et al.American Journal of Medical Genetics|March 31, 1997
Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophyJ Berger, B Löschl, H Bernheimer, et al.Pageof 854