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D Chitayat

Showing results (81-90 of 211) with videos related to

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American Journal of Medical Genetics|November 7, 1998
Familial growth hormone deficiency associated with MRI abnormalitiesJ Hamilton, D Chitayat, S Blaser, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|September 11, 1998
Otocephaly: prenatal sonographic diagnosisR Rahmani, M Dixon, D Chitayat, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetusD Chitayat, A Balbul, V Hani, et al.
Clinical Genetics|March 1, 1989
Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feetD Chitayat, E B Davis, B C McGillivray, et al.
Prenatal Diagnosis|September 1, 1995
The prognostic factors in the prenatal diagnosis of the echogenic fetal lungJ Barret, D Chitayat, M Sermer, et al.
American Journal of Medical Genetics|September 1, 1990
Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibsD Chitayat, J G Hall, R M Couch, et al.
Pediatric Radiology|December 1, 2001
New dysplasia or achondrogenesis type 1B? The importance of histology and molecular biology in delineating skeletal dysplasiasS Unger, M Le Merrer, P Meinecke, et al.
Clinical Genetics|October 27, 1998
Severe classical congenital muscular dystrophy and merosin expressionJ Vajsar, D Chitayat, L E Becker, et al.
American Journal of Medical Genetics|April 1, 1991
Lethal congenital muscular dystrophy with cataracts and a minor brain anomaly: new entity or variant of Walker-Warburg syndrome?D S Wargowski, D Chitayat, R W Tyson, et al.
Journal of Pediatric Hematology/Oncology|December 22, 1999
Juvenile myelomonocytic leukemia and Noonan syndromeK Choong, M H Freedman, D Chitayat, et al.
Pageof 22

Showing results (81-90 of 211) with videos related to

Sort By:
Pageof 22
American Journal of Medical Genetics|November 7, 1998
Familial growth hormone deficiency associated with MRI abnormalitiesJ Hamilton, D Chitayat, S Blaser, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|September 11, 1998
Otocephaly: prenatal sonographic diagnosisR Rahmani, M Dixon, D Chitayat, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetusD Chitayat, A Balbul, V Hani, et al.
Clinical Genetics|March 1, 1989
Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feetD Chitayat, E B Davis, B C McGillivray, et al.
Prenatal Diagnosis|September 1, 1995
The prognostic factors in the prenatal diagnosis of the echogenic fetal lungJ Barret, D Chitayat, M Sermer, et al.
American Journal of Medical Genetics|September 1, 1990
Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibsD Chitayat, J G Hall, R M Couch, et al.
Pediatric Radiology|December 1, 2001
New dysplasia or achondrogenesis type 1B? The importance of histology and molecular biology in delineating skeletal dysplasiasS Unger, M Le Merrer, P Meinecke, et al.
Clinical Genetics|October 27, 1998
Severe classical congenital muscular dystrophy and merosin expressionJ Vajsar, D Chitayat, L E Becker, et al.
American Journal of Medical Genetics|April 1, 1991
Lethal congenital muscular dystrophy with cataracts and a minor brain anomaly: new entity or variant of Walker-Warburg syndrome?D S Wargowski, D Chitayat, R W Tyson, et al.
Journal of Pediatric Hematology/Oncology|December 22, 1999
Juvenile myelomonocytic leukemia and Noonan syndromeK Choong, M H Freedman, D Chitayat, et al.
Pageof 22