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D Chitayat

Showing results (31-40 of 211) with videos related to

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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
Blood|October 7, 2000
A partial deficiency of interleukin-7R alpha is sufficient to abrogate T-cell development and cause severe combined immunodeficiencyC M Roifman, J Zhang, D Chitayat, et al.
Obstetrics and Gynecology|October 1, 1995
Spectrophotometry of amniotic fluid: a simple and rapid method for distinguishing between gestational sacs in second-trimester amniocentesis of twin pregnanciesD Chitayat, G Ohel, R Marion, et al.
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.
American Journal of Medical Genetics|October 1, 1988
Congenital abnormalities in two sibs exposed to valproic acid in uteroD Chitayat, K Farrell, L Anderson, et al.
Pediatric Neurology|March 30, 2000
Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndromeJ Vajsar, C Ackerley, D Chitayat, et al.
American Journal of Medical Genetics|February 1, 1992
Ebstein anomaly: report of a familial occurrence and prenatal diagnosisN McIntosh, D Chitayat, M Bardanis, et al.
Pageof 22

Showing results (31-40 of 211) with videos related to

Sort By:
Pageof 22
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
Blood|October 7, 2000
A partial deficiency of interleukin-7R alpha is sufficient to abrogate T-cell development and cause severe combined immunodeficiencyC M Roifman, J Zhang, D Chitayat, et al.
Obstetrics and Gynecology|October 1, 1995
Spectrophotometry of amniotic fluid: a simple and rapid method for distinguishing between gestational sacs in second-trimester amniocentesis of twin pregnanciesD Chitayat, G Ohel, R Marion, et al.
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.
American Journal of Medical Genetics|October 1, 1988
Congenital abnormalities in two sibs exposed to valproic acid in uteroD Chitayat, K Farrell, L Anderson, et al.
Pediatric Neurology|March 30, 2000
Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndromeJ Vajsar, C Ackerley, D Chitayat, et al.
American Journal of Medical Genetics|February 1, 1992
Ebstein anomaly: report of a familial occurrence and prenatal diagnosisN McIntosh, D Chitayat, M Bardanis, et al.
Pageof 22