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William Reardon

Showing results (11-20 of 68) with videos related to

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Pediatric Surgery International|February 18, 2006
Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patientsMudaffer Al-Mudaffer, Prem Puri, William Reardon
Cardiology in the Young|June 4, 2015
Response to commentary: biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiencyRanjana Dhar, William Reardon, Colin J McMahon
Clinical Dysmorphology|February 2, 2002
Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndromeOrla G Killeen, Peter Kelehan, William Reardon
Cardiology in the Young|July 16, 2014
Biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiencyRanjana Dhar, William Reardon, Colin J McMahon
Obstetrics and Gynecology|February 3, 2007
Unexplained prelabor uterine rupture in a term primigravidaColin A Walsh, William Reardon, Michael E Foley
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 16, 2007
Bilateral optic disk swelling in the 4q34 deletion syndromePaul Connell, Donal Brosnahan, Adam Dunlop, et al.
Clinical Dysmorphology|June 7, 2007
Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome)Patricia Foley, Fionnuala McAuliffe, Marice Mullarkey, et al.
Clinical Dysmorphology|June 11, 2008
Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndromeRaveen Shahdadpuri, Anne O'Meara, Maureen O'Sullivan, et al.
Clinical Dysmorphology|July 19, 2003
Congenital ptosis with esotropia in brothersAsha Latha Madasseri, Paul Mullaney, Colm Costigan, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
Deafness associated with bilateral facial diplegia, ptosis and hypermobile joints--A new autosomal recessive condition?William Reardon, Mairead McGinn, Mary D King, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Pediatric Surgery International|February 18, 2006
Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patientsMudaffer Al-Mudaffer, Prem Puri, William Reardon
Cardiology in the Young|June 4, 2015
Response to commentary: biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiencyRanjana Dhar, William Reardon, Colin J McMahon
Clinical Dysmorphology|February 2, 2002
Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndromeOrla G Killeen, Peter Kelehan, William Reardon
Cardiology in the Young|July 16, 2014
Biventricular non-compaction hypertrophic cardiomyopathy in association with congenital complete heart block and type I mitochondrial complex deficiencyRanjana Dhar, William Reardon, Colin J McMahon
Obstetrics and Gynecology|February 3, 2007
Unexplained prelabor uterine rupture in a term primigravidaColin A Walsh, William Reardon, Michael E Foley
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 16, 2007
Bilateral optic disk swelling in the 4q34 deletion syndromePaul Connell, Donal Brosnahan, Adam Dunlop, et al.
Clinical Dysmorphology|June 7, 2007
Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome)Patricia Foley, Fionnuala McAuliffe, Marice Mullarkey, et al.
Clinical Dysmorphology|June 11, 2008
Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndromeRaveen Shahdadpuri, Anne O'Meara, Maureen O'Sullivan, et al.
Clinical Dysmorphology|July 19, 2003
Congenital ptosis with esotropia in brothersAsha Latha Madasseri, Paul Mullaney, Colm Costigan, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
Deafness associated with bilateral facial diplegia, ptosis and hypermobile joints--A new autosomal recessive condition?William Reardon, Mairead McGinn, Mary D King, et al.
Pageof 7