Showing results (181-190 of 337) with videos related to
Sort By:
Pageof 34
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.American Journal of Diseases of Children (1960)|January 1, 1987
Targeted early childhood programming. The promise half fulfilledJ S Palfrey, D K Walker, M Sullivan, et al.The Journal of Pediatrics|January 1, 1975
The medical ethics of bone marrow transplantation in childhoodM D Levine, B M Camitta, D Nathan, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|November 23, 2001
Attentional function as measured by a Continuous Performance Task in children with dyscalculiaR L Lindsay, T Tomazic, M D Levine, et al.American Journal of Diseases of Children (1960)|July 1, 1979
Training in developmental pediatrics. How practitioners perceive the gapP H Dworkin, J P Shonkoff, A Leviton, et al.Clinical Pediatrics|November 1, 1979
Chronic and occult stool retention: a clinical tool for its evaluation in school-aged childrenR G Barr, M D Levine, R H Wilkinson, et al.Prenatal Diagnosis|November 1, 1993
Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variabilityC A Bacino, L D Platt, A Garber, et al.The Journal of Biological Chemistry|March 21, 1998
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutationM A Weis, D J Wilkin, H J Kim, et al.American Journal of Medical Genetics|July 1, 1990
Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusionsM Frydman, J Bar-Ziv, R Preminger-Shapiro, et al.Pageof 34