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David Chitayat

Showing results (141-150 of 353) with videos related to

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Prenatal Diagnosis|January 21, 2003
Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletionCatherine Barrea, Shi-Joon Yoo, David Chitayat, et al.
American Journal of Medical Genetics. Part A|November 7, 2013
Hand and fibrillin-1 deposition abnormalities in Loeys-Dietz syndrome--expanding the clinical spectrumBrian H Y Chung, Tim Bradley, Lars Grosse-Wortmann, et al.
Molecular Human Reproduction|August 1, 2002
Expression of cystic fibrosis transmembrane conductance regulator during early human embryo developmentAvraham Ben-Chetrit, Monica Antenos, Andrea Jurisicova, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Central nervous system abnormalities in two cases with neonatal Marfan syndrome with novel mutations in the fibrillin-1 geneChristopher P Barnett, Gregory J Wilson, David A Chiasson, et al.
Prenatal Diagnosis|October 18, 2008
Prospective experience with integrated prenatal screening and first trimester combined screening for trisomy 21 in a large Canadian urban centerNanette Okun, Anne M Summers, Barry Hoffman, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|October 5, 2007
Maternal luteoma of pregnancy presenting with virilization of the female infantRachel F Spitzer, Diane Wherrett, David Chitayat, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Clinical and genetic aspects of trigonocephaly: a study of 25 casesCyrus Azimi, Shelley J Kennedy, David Chitayat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2013
Risk estimates for complex disorders: comparing personal genome testing and family historyLila Aiyar, Cheryl Shuman, Robin Hayeems, et al.
Prenatal Diagnosis|March 22, 2023
Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcomeEran Ashwal, Susan Blaser, Ashley Leckie, et al.
American Journal of Medical Genetics. Part A|May 29, 2013
Broadening the ciliopathy spectrum: motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 geneSharon Moalem, Sarah Keating, Patrick Shannon, et al.
Pageof 36

Showing results (141-150 of 353) with videos related to

Sort By:
Pageof 36
Prenatal Diagnosis|January 21, 2003
Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletionCatherine Barrea, Shi-Joon Yoo, David Chitayat, et al.
American Journal of Medical Genetics. Part A|November 7, 2013
Hand and fibrillin-1 deposition abnormalities in Loeys-Dietz syndrome--expanding the clinical spectrumBrian H Y Chung, Tim Bradley, Lars Grosse-Wortmann, et al.
Molecular Human Reproduction|August 1, 2002
Expression of cystic fibrosis transmembrane conductance regulator during early human embryo developmentAvraham Ben-Chetrit, Monica Antenos, Andrea Jurisicova, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Central nervous system abnormalities in two cases with neonatal Marfan syndrome with novel mutations in the fibrillin-1 geneChristopher P Barnett, Gregory J Wilson, David A Chiasson, et al.
Prenatal Diagnosis|October 18, 2008
Prospective experience with integrated prenatal screening and first trimester combined screening for trisomy 21 in a large Canadian urban centerNanette Okun, Anne M Summers, Barry Hoffman, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|October 5, 2007
Maternal luteoma of pregnancy presenting with virilization of the female infantRachel F Spitzer, Diane Wherrett, David Chitayat, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Clinical and genetic aspects of trigonocephaly: a study of 25 casesCyrus Azimi, Shelley J Kennedy, David Chitayat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2013
Risk estimates for complex disorders: comparing personal genome testing and family historyLila Aiyar, Cheryl Shuman, Robin Hayeems, et al.
Prenatal Diagnosis|March 22, 2023
Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcomeEran Ashwal, Susan Blaser, Ashley Leckie, et al.
American Journal of Medical Genetics. Part A|May 29, 2013
Broadening the ciliopathy spectrum: motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 geneSharon Moalem, Sarah Keating, Patrick Shannon, et al.
Pageof 36