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American Journal of Diseases of Children (1960)|November 1, 1993
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotypeS D McLean, H M Saal, N B Spinner, et al.American Journal of Medical Genetics|October 28, 1997
Thoracic tumors in children with neurofibromatosis-1E K Schorry, A H Crawford, J C Egelhoff, et al.American Journal of Medical Genetics|November 15, 1993
Brachmann-de Lange syndrome with normal IQH M Saal, C A Samango-Sprouse, L A Rodnan, et al.Prenatal Diagnosis|November 1, 1992
Cystic hygroma and congenital diaphragmatic hernia: early prenatal sonographic evaluation of Fryns' syndromeD I Bulas, H M Saal, J F Allen, et al.American Journal of Medical Genetics|June 27, 1997
New insights into the phenotypes of 6q deletionsR J Hopkin, E Schorry, M Bofinger, et al.American Journal of Medical Genetics|July 17, 1995
Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skullH M Saal, D I Bulas, J F Allen, et al.American Journal of Medical Genetics|December 22, 1999
Variation in microdeletions of the cyclic AMP-responsive element-binding protein gene at chromosome band 16p13.3 in the Rubinstein-Taybi syndromeR I Blough, F Petrij, J G Dauwerse, et al.American Journal of Medical Genetics|May 26, 1998
Partial trisomy 1q with growth hormone deficiency and normal intelligenceE K Schorry, K N Dietrich, H M Saal, et al.American Journal of Medical Genetics|December 30, 1996
Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2H M Saal, L J King, D Zimmerman, et al.Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.Pageof 4