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Pediatrics|April 1, 1990
Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasiaC Cunniff, K L Jones, H M Saal, et al.The Journal of Pediatrics|August 10, 2000
Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndromeR J Hopkin, E K Schorry, M Bofinger, et al.The Journal of Pediatrics|June 4, 1999
Social and emotional problems in children with neurofibromatosis type 1: evidence and proposed interventionsN S Johnson, H M Saal, A M Lovell, et al.American Journal of Medical Genetics|July 1, 1988
Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomaliesH M Saal, R M Greenstein, P J Weinbaum, et al.Prenatal Diagnosis|September 1, 1996
Prenatal diagnosis of ring chromosome 6 in a fetus with hydrocephalusM E Walker, D A Lynch-Salamon, A Milatovich, et al.Journal of Medical Genetics|December 14, 1999
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32M M Lees, R M Winter, S Malcolm, et al.Obstetrics and Gynecology|October 1, 1987
Cytogenetic evaluation of fetal death: the role of amniocentesisH M Saal, J Rodis, P J Weinbaum, et al.American Journal of Medical Genetics|July 15, 1992
Dominant syndrome with isolated cryptophthalmos and ocular anomaliesH M Saal, E I Traboulsi, P Gavaris, et al.Clinical Genetics|April 1, 1988
Diploid/tetraploid mosaicism in a liveborn infant demonstrable only in the bone marrow: case report and literature reviewD J Aughton, H M Saal, J A Delach, et al.The New England Journal of Medicine|August 6, 1987
Screening for fetal Down's syndrome in pregnancy by measuring maternal serum alpha-fetoprotein levelsM S DiMaio, A Baumgarten, R M Greenstein, et al.Pageof 4