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Pradeep C Vasudevan

Showing results (1-10 of 31) with videos related to

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Clinical Medicine (London, England)|April 8, 2018
ResponsePradeep C Vasudevan, Mohnish Suri
Clinical Dysmorphology|June 15, 2004
A case of Fryns syndrome without diaphragmatic hernia and review of the literaturePradeep C Vasudevan, Helen Stewart
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 19, 2013
Status epilepsy in CCM with KRIT1 gene changeEmily V Craft, Pradeep C Vasudevan
Clinical Dysmorphology|August 5, 2015
Is 15q11.2 microdeletion associated with periventricular nodular heterotopia?Jessica A Radley, Pradeep C Vasudevan
Clinical Dysmorphology|March 15, 2006
Monosomy 5p and trisomy 12p in a boy with familial balanced translocationPradeep C Vasudevan, Michael J Parker
Clinical Dysmorphology|March 14, 2007
Prader-Willi and Klinefelter syndrome: a coincidence or not?Pradeep C Vasudevan, Oliver W J Quarrell
Prenatal Diagnosis|October 3, 2015
Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literatureGabriela E Jones, Hatem A Mousa, Helen Rowley, et al.
Ophthalmic Genetics|February 11, 2016
14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disabilityGabriela E Jones, Lisa Robertson, Paul Warman, et al.
Clinical Dysmorphology|May 22, 2012
Hypertelorism, radial ray defects, dextrocardia, hypoplastic ribs and renal anomaly: report of a second case and confirmation of the phenotypeGabriela E Fuchs, Mohnish Suri, Anthony Dux, et al.
Prenatal Diagnosis|February 2, 2006
The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literaturePradeep C Vasudevan, Marta C Cohen, Elspeth H Whitby, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Clinical Medicine (London, England)|April 8, 2018
ResponsePradeep C Vasudevan, Mohnish Suri
Clinical Dysmorphology|June 15, 2004
A case of Fryns syndrome without diaphragmatic hernia and review of the literaturePradeep C Vasudevan, Helen Stewart
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 19, 2013
Status epilepsy in CCM with KRIT1 gene changeEmily V Craft, Pradeep C Vasudevan
Clinical Dysmorphology|August 5, 2015
Is 15q11.2 microdeletion associated with periventricular nodular heterotopia?Jessica A Radley, Pradeep C Vasudevan
Clinical Dysmorphology|March 15, 2006
Monosomy 5p and trisomy 12p in a boy with familial balanced translocationPradeep C Vasudevan, Michael J Parker
Clinical Dysmorphology|March 14, 2007
Prader-Willi and Klinefelter syndrome: a coincidence or not?Pradeep C Vasudevan, Oliver W J Quarrell
Prenatal Diagnosis|October 3, 2015
Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literatureGabriela E Jones, Hatem A Mousa, Helen Rowley, et al.
Ophthalmic Genetics|February 11, 2016
14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disabilityGabriela E Jones, Lisa Robertson, Paul Warman, et al.
Clinical Dysmorphology|May 22, 2012
Hypertelorism, radial ray defects, dextrocardia, hypoplastic ribs and renal anomaly: report of a second case and confirmation of the phenotypeGabriela E Fuchs, Mohnish Suri, Anthony Dux, et al.
Prenatal Diagnosis|February 2, 2006
The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literaturePradeep C Vasudevan, Marta C Cohen, Elspeth H Whitby, et al.
Pageof 4