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Pediatric Surgery International
|
February 18, 2006
Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients
Mudaffer 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 deficiency
Ranjana 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 syndrome
Orla 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 deficiency
Ranjana Dhar, William Reardon, Colin J McMahon
Obstetrics and Gynecology
|
February 3, 2007
Unexplained prelabor uterine rupture in a term primigravida
Colin 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 syndrome
Paul 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 syndrome
Raveen Shahdadpuri, Anne O'Meara, Maureen O'Sullivan, et al.
Clinical Dysmorphology
|
July 19, 2003
Congenital ptosis with esotropia in brothers
Asha 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.
Page
of 7
Search research articles
Search
Showing results (11-20 of 68) with videos related to
Sort By:
Page
of 7
Pediatric Surgery International
|
February 18, 2006
Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients
Mudaffer 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 deficiency
Ranjana 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 syndrome
Orla 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 deficiency
Ranjana Dhar, William Reardon, Colin J McMahon
Obstetrics and Gynecology
|
February 3, 2007
Unexplained prelabor uterine rupture in a term primigravida
Colin 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 syndrome
Paul 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 syndrome
Raveen Shahdadpuri, Anne O'Meara, Maureen O'Sullivan, et al.
Clinical Dysmorphology
|
July 19, 2003
Congenital ptosis with esotropia in brothers
Asha 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.
Page
of 7