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David Chitayat

Showing results (131-140 of 353) with videos related to

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Archives of Disease in Childhood. Fetal and Neonatal Edition|April 14, 2026
Diagnostic yield and imaging: aetiology correlations in prenatal intracranial haemorrhage-a retrospective cohort studyShiri Shinar, Laurence S Carmant, Priya Tripathy, et al.
Prenatal Diagnosis|June 17, 2025
Occipital Cephalocele, Polymicrogyria, Ocular Anomaly and Vermian Dysplasia: Prenatal Markers for Knobloch SyndromeLaurence Sophie Carmant, Elka Miller, David Chitayat, et al.
Human Molecular Genetics|November 4, 2010
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissuesArturo López Castel, Masayuki Nakamori, Stephanie Tomé, et al.
The Lancet. Oncology|October 26, 2010
Breast and ovarian cancer: Y do we forget about dad?Jeanna M McCuaig, Celia Greenwood, Cheryl Shuman, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndromeJane Gillis, Elena Burashnikov, Charles Antzelevitch, et al.
Pediatric Radiology|July 18, 2008
MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlationAshley J Robinson, Susan Blaser, Ants Toi, et al.
The Journal of Pediatrics|November 15, 2003
Fetal rhabdomyoma: prenatal diagnosis, clinical outcome, and incidence of associated tuberous sclerosis complexRima S Bader, David Chitayat, Edmond Kelly, et al.
Prenatal Diagnosis|May 3, 2025
KIDINS220 Variant Associated With Hypoplasia of the Corpus Callosum and Aqueduct StenosisKimia Ghannad-Zadeh, Patrick Shannon, Rebekah Jobling, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplicationSharon Moalem, Riyana Babul-Hirji, Dmitri J Stavropolous, et al.
The Annals of Thoracic Surgery|January 23, 2013
Unexpected contained rupture of a ductus arteriosus aneurysm found at surgical repair in an infant with Loeys-Dietz syndromeFrederic Jacques, Lars Grosse-Wortmann, Edward J Hickey, et al.
Pageof 36

Showing results (131-140 of 353) with videos related to

Sort By:
Pageof 36
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 14, 2026
Diagnostic yield and imaging: aetiology correlations in prenatal intracranial haemorrhage-a retrospective cohort studyShiri Shinar, Laurence S Carmant, Priya Tripathy, et al.
Prenatal Diagnosis|June 17, 2025
Occipital Cephalocele, Polymicrogyria, Ocular Anomaly and Vermian Dysplasia: Prenatal Markers for Knobloch SyndromeLaurence Sophie Carmant, Elka Miller, David Chitayat, et al.
Human Molecular Genetics|November 4, 2010
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissuesArturo López Castel, Masayuki Nakamori, Stephanie Tomé, et al.
The Lancet. Oncology|October 26, 2010
Breast and ovarian cancer: Y do we forget about dad?Jeanna M McCuaig, Celia Greenwood, Cheryl Shuman, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndromeJane Gillis, Elena Burashnikov, Charles Antzelevitch, et al.
Pediatric Radiology|July 18, 2008
MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlationAshley J Robinson, Susan Blaser, Ants Toi, et al.
The Journal of Pediatrics|November 15, 2003
Fetal rhabdomyoma: prenatal diagnosis, clinical outcome, and incidence of associated tuberous sclerosis complexRima S Bader, David Chitayat, Edmond Kelly, et al.
Prenatal Diagnosis|May 3, 2025
KIDINS220 Variant Associated With Hypoplasia of the Corpus Callosum and Aqueduct StenosisKimia Ghannad-Zadeh, Patrick Shannon, Rebekah Jobling, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplicationSharon Moalem, Riyana Babul-Hirji, Dmitri J Stavropolous, et al.
The Annals of Thoracic Surgery|January 23, 2013
Unexpected contained rupture of a ductus arteriosus aneurysm found at surgical repair in an infant with Loeys-Dietz syndromeFrederic Jacques, Lars Grosse-Wortmann, Edward J Hickey, et al.
Pageof 36