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R Savarirayan

Showing results (1-10 of 44) with videos related to

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Pediatric Radiology|June 26, 1999
Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)R Savarirayan
Journal of Paediatrics and Child Health|April 1, 1997
Megaloblastic anaemia and pancytopenia secondary to prophylactic cotrimoxazole therapyH Tapp, R Savarirayan
Journal of Medical Genetics|July 25, 1998
Acampomelic campomelic dysplasia with de novo 5q;17q reciprocal translocation and severe phenotypeR Savarirayan, A Bankier
Journal of Medical Genetics|July 29, 1999
Simpson-Golabi-Behmel syndrome and attention deficit hyperactivity disorder in two brothersR Savarirayan, A Bankier
American Journal of Medical Genetics|December 18, 2001
Intermediate form of ablepharon-macrostomia syndrome with CNS abnormalitiesD J Amor, R Savarirayan
Clinical Dysmorphology|April 1, 1997
Craniosynostosis in Roberts syndromeR Savarirayan, E M Thompson
Journal of Medical Genetics|September 11, 1998
Baller-Gerold syndrome associated with congenital portal venous malformationR Savarirayan, P Tomlinson, E Thompson
Archives of Disease in Childhood|September 23, 2003
Genetic counselling after carrier detection by newborn screening when one parent carries DeltaF508 and the other R117HL Curnow, R Savarirayan, J Massie
American Journal of Medical Genetics|March 8, 2000
Molecular diagnosis of Stickler syndrome: a COL2A1 stop codon mutation screening strategy that is not compromised by mutant mRNA instabilityS Freddi, R Savarirayan, J F Bateman
Nephrologie|March 17, 2004
Ossifying fibroma of the face and hyperparathyroidism in a chronic hemodialysis patientM J Aldred, A A Talacko, R Savarirayan
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Pediatric Radiology|June 26, 1999
Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)R Savarirayan
Journal of Paediatrics and Child Health|April 1, 1997
Megaloblastic anaemia and pancytopenia secondary to prophylactic cotrimoxazole therapyH Tapp, R Savarirayan
Journal of Medical Genetics|July 25, 1998
Acampomelic campomelic dysplasia with de novo 5q;17q reciprocal translocation and severe phenotypeR Savarirayan, A Bankier
Journal of Medical Genetics|July 29, 1999
Simpson-Golabi-Behmel syndrome and attention deficit hyperactivity disorder in two brothersR Savarirayan, A Bankier
American Journal of Medical Genetics|December 18, 2001
Intermediate form of ablepharon-macrostomia syndrome with CNS abnormalitiesD J Amor, R Savarirayan
Clinical Dysmorphology|April 1, 1997
Craniosynostosis in Roberts syndromeR Savarirayan, E M Thompson
Journal of Medical Genetics|September 11, 1998
Baller-Gerold syndrome associated with congenital portal venous malformationR Savarirayan, P Tomlinson, E Thompson
Archives of Disease in Childhood|September 23, 2003
Genetic counselling after carrier detection by newborn screening when one parent carries DeltaF508 and the other R117HL Curnow, R Savarirayan, J Massie
American Journal of Medical Genetics|March 8, 2000
Molecular diagnosis of Stickler syndrome: a COL2A1 stop codon mutation screening strategy that is not compromised by mutant mRNA instabilityS Freddi, R Savarirayan, J F Bateman
Nephrologie|March 17, 2004
Ossifying fibroma of the face and hyperparathyroidism in a chronic hemodialysis patientM J Aldred, A A Talacko, R Savarirayan
Pageof 5