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American Journal of Human Genetics|October 1, 1995
The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32S Brown, J Russo, D Chitayat, et al.
American Journal of Medical Genetics|July 1, 1989
Lymphatic abnormalities in fetuses with posterior cervical cystic hygromaD Chitayat, D K Kalousek, J S Bamforth
Acta Paediatrica Scandinavica|July 1, 1985
Pseudohypoaldosteronism in a female infant and her family: diversity of clinical expression and mode of inheritanceD Chitayat, Z Spirer, D Ayalon, et al.
American Journal of Medical Genetics|November 15, 1992
Autosomal recessive oral-facial-digital syndrome with resemblance to OFD types II, III, IV and VI: a new OFD syndrome?D Chitayat, H J Stalker, E M Azouz
American Journal of Medical Genetics|February 1, 1992
Intrafamilial variability in cleidocranial dysplasia: a three generation familyD Chitayat, K A Hodgkinson, E M Azouz
American Journal of Medical Genetics|March 1, 1990
Hypomelanosis of Ito--a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicismD Chitayat, J M Friedman, M M Johnston
Biochemistry|May 31, 1994
Effect of divalent cations on the molecular structure of the GroEL oligomerA Azem, S Diamant, P Goloubinoff
American Journal of Diseases of Children (1960)|December 1, 1990
Midfacial hypoplasia associated with long-term intubation for bronchopulmonary dysplasiaA Rotschild, P J Dison, D Chitayat, et al.
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