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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1985
Nonrandom association of a type II procollagen genotype with achondroplasiaC E Eng, R M Pauli, C M StromAmerican Journal of Public Health|September 1, 1987
Accuracy of fetal death reports: comparison with data from an independent stillbirth assessment programA E Greb, R M Pauli, R S KirbyCytogenetics and Cell Genetics|January 1, 1984
A human lymphoblastoid cell line from the offspring of a brother-sister matingE A Azen, R C Karn, R M PauliAmerican Journal of Diseases of Children (1960)|November 1, 1983
'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletionR M Pauli, L F Meisner, R J SzmandaAmerican Journal of Medical Genetics|May 1, 1990
Fetal disruptions: assessment of frequency, heterogeneity, and embryologic mechanisms in a population referred to a community-based stillbirth assessment programH J Luebke, C A Reiser, R M PauliJournal of Pediatric Orthopedics|May 1, 1985
Hand-reduction malformations: genetic and syndromic analysisR T Pilarski, R M Pauli, W D EngberClinical Genetics|June 1, 1985
Familial recurrence of terminal transverse defects of the armR M Pauli, R M Lebovitz, R D MeyerAmerican Journal of Medical Genetics|July 1, 1990
Temperament in Williams syndromeS A Tomc, N K Williamson, R M PauliClinical Dysmorphology|July 1, 1995
Patterson-Lowry rhizomelic dysplasia: a possible second exampleM S Williams, K D Josephson, R M PauliAmerican Journal of Medical Genetics|October 1, 1984
Achondroplasia: unexpected familial recurrenceC A Reiser, R M Pauli, J G HallPageof 31