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D Chitayat

Showing results (141-150 of 211) with videos related to

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The Journal of Pediatrics|July 1, 1988
Trisomy 18 score: a rapid, reliable diagnostic test for trisomy 18R W Marion, D Chitayat, R G Hutcheon, et al.
Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 15, 2008
Rhombencephalosynapsis: prenatal imaging and autopsy findingsF McAuliffe, D Chitayat, W Halliday, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 11, 2010
Fetal forehead hemangiopericytoma: prenatal diagnosis and postnatal outcomeH Y B Chung, L Chu, C Forrest, et al.
American Journal of Medical Genetics|January 16, 1995
Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literatureD Chitayat, R H Ruvalcaba, R Babul, et al.
Human Biology|February 1, 1993
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of QuebecC Dionne, C Gagné, P Julien, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
American Journal of Medical Genetics|March 1, 1990
Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?D Chitayat, B C McGillivray, R Rothstein, et al.
Genomics|June 21, 2001
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutationsM Li, J Squire, C Shuman, et al.
American Journal of Medical Genetics|June 9, 1999
Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcomeD Chitayat, B Fernandez, A Gardner, et al.
Pageof 22

Showing results (141-150 of 211) with videos related to

Sort By:
Pageof 22
The Journal of Pediatrics|July 1, 1988
Trisomy 18 score: a rapid, reliable diagnostic test for trisomy 18R W Marion, D Chitayat, R G Hutcheon, et al.
Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 15, 2008
Rhombencephalosynapsis: prenatal imaging and autopsy findingsF McAuliffe, D Chitayat, W Halliday, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 11, 2010
Fetal forehead hemangiopericytoma: prenatal diagnosis and postnatal outcomeH Y B Chung, L Chu, C Forrest, et al.
American Journal of Medical Genetics|January 16, 1995
Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literatureD Chitayat, R H Ruvalcaba, R Babul, et al.
Human Biology|February 1, 1993
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of QuebecC Dionne, C Gagné, P Julien, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
American Journal of Medical Genetics|March 1, 1990
Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?D Chitayat, B C McGillivray, R Rothstein, et al.
Genomics|June 21, 2001
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutationsM Li, J Squire, C Shuman, et al.
American Journal of Medical Genetics|June 9, 1999
Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcomeD Chitayat, B Fernandez, A Gardner, et al.
Pageof 22