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David Chitayat

Showing results (241-250 of 354) with videos related to

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American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 6, 2010
Prenatal exposure to mycophenolate mofetil: an updated estimateChagit Klieger-Grossmann, David Chitayat, Sharon Lavign, et al.
The Journal of Clinical Psychiatry|August 5, 2021
Reproductive Safety of Second-Generation Antipsychotics: Updated Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsAdele C Viguera, Marlene P Freeman, Lina Góez-Mogollón, et al.
Fetal Diagnosis and Therapy|January 19, 2026
The Evolution of Cephalocentesis in Contemporary Obstetric Practice: From Emergency Intervention to Planned ProcedureCatherine Windrim, Yada Kunpalin, Alyaa AlRefai, et al.
American Journal of Medical Genetics. Part A|October 26, 2023
45,X/46,XY mosaicism: Clinical manifestations and long term follow-upEbba Alkhunaizi, Jenna Plamondon Albrecht, Mahmoud Aarabi, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric populationBita Hashemi, Anne Bassett, David Chitayat, et al.
American Journal of Human Genetics|March 6, 2012
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signalingAmy E Merrill, Anna Sarukhanov, Pavel Krejci, et al.
The American Journal of Psychiatry|October 7, 2015
Reproductive Safety of Second-Generation Antipsychotics: Current Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsLee S Cohen, Adele C Viguera, Kathryn A McInerney, et al.
American Journal of Medical Genetics. Part A|January 18, 2019
Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrumEbba Alkhunaizi, Shirley Shuster, Patrick Shannon, et al.
Cellular and Molecular Gastroenterology and Hepatology|July 25, 2015
Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and HypertriglyceridemiaAbdul Elkadri, Cornelia Thoeni, Sophie J Deharvengt, et al.
Pageof 36

Showing results (241-250 of 354) with videos related to

Sort By:
Pageof 36
American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 6, 2010
Prenatal exposure to mycophenolate mofetil: an updated estimateChagit Klieger-Grossmann, David Chitayat, Sharon Lavign, et al.
The Journal of Clinical Psychiatry|August 5, 2021
Reproductive Safety of Second-Generation Antipsychotics: Updated Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsAdele C Viguera, Marlene P Freeman, Lina Góez-Mogollón, et al.
Fetal Diagnosis and Therapy|January 19, 2026
The Evolution of Cephalocentesis in Contemporary Obstetric Practice: From Emergency Intervention to Planned ProcedureCatherine Windrim, Yada Kunpalin, Alyaa AlRefai, et al.
American Journal of Medical Genetics. Part A|October 26, 2023
45,X/46,XY mosaicism: Clinical manifestations and long term follow-upEbba Alkhunaizi, Jenna Plamondon Albrecht, Mahmoud Aarabi, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric populationBita Hashemi, Anne Bassett, David Chitayat, et al.
American Journal of Human Genetics|March 6, 2012
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signalingAmy E Merrill, Anna Sarukhanov, Pavel Krejci, et al.
The American Journal of Psychiatry|October 7, 2015
Reproductive Safety of Second-Generation Antipsychotics: Current Data From the Massachusetts General Hospital National Pregnancy Registry for Atypical AntipsychoticsLee S Cohen, Adele C Viguera, Kathryn A McInerney, et al.
American Journal of Medical Genetics. Part A|January 18, 2019
Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrumEbba Alkhunaizi, Shirley Shuster, Patrick Shannon, et al.
Cellular and Molecular Gastroenterology and Hepatology|July 25, 2015
Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and HypertriglyceridemiaAbdul Elkadri, Cornelia Thoeni, Sophie J Deharvengt, et al.
Pageof 36