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A K Iafolla

Showing results (1-10 of 12) with videos related to

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Journal of Perinatology : Official Journal of the California Perinatal Association|March 1, 1995
Medicinal leeches in the postoperative care of bladder exstrophyA K Iafolla
Clinics in Perinatology|December 1, 1990
Prenatal diagnosis of metabolic diseaseA K Iafolla, A McConkie-Rosell
Journal of Genetic Counseling|November 19, 2013
Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counselingA McConkie-Rosell, A K Iafolla
American Journal of Medical Genetics|January 1, 1991
VATER and hydrocephalus: distinct syndrome?A K Iafolla, A McConkie-Rosell, Y T Chen
The Journal of Pediatrics|March 1, 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected childrenA K Iafolla, R J Thompson, C R Roe
Pediatric Pulmonology|September 1, 1995
Familial infantile apnea and immature beta oxidationA K Iafolla, I B Browning, C R Roe
Journal of Medical Genetics|July 1, 1996
A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisitedN Helali, A K Iafolla, S G Kahler, et al.
American Journal of Medical Genetics|November 20, 1995
Fryns syndrome survivors and neurologic outcomeJ L Van Hove, G A Spiridigliozzi, R Heinz, et al.
American Journal of Medical Genetics|October 23, 1995
Hemangioma, supraumbilical midline raphé, and coarctation of the aorta with a right aortic arch: single causal entity?P Kishnani, A K Iafolla, A McConkie-Rosell, et al.
American Journal of Medical Genetics|September 11, 1992
Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literatureJ L Van Hove, A McConkie-Rosell, Y T Chen, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Perinatology : Official Journal of the California Perinatal Association|March 1, 1995
Medicinal leeches in the postoperative care of bladder exstrophyA K Iafolla
Clinics in Perinatology|December 1, 1990
Prenatal diagnosis of metabolic diseaseA K Iafolla, A McConkie-Rosell
Journal of Genetic Counseling|November 19, 2013
Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counselingA McConkie-Rosell, A K Iafolla
American Journal of Medical Genetics|January 1, 1991
VATER and hydrocephalus: distinct syndrome?A K Iafolla, A McConkie-Rosell, Y T Chen
The Journal of Pediatrics|March 1, 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected childrenA K Iafolla, R J Thompson, C R Roe
Pediatric Pulmonology|September 1, 1995
Familial infantile apnea and immature beta oxidationA K Iafolla, I B Browning, C R Roe
Journal of Medical Genetics|July 1, 1996
A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisitedN Helali, A K Iafolla, S G Kahler, et al.
American Journal of Medical Genetics|November 20, 1995
Fryns syndrome survivors and neurologic outcomeJ L Van Hove, G A Spiridigliozzi, R Heinz, et al.
American Journal of Medical Genetics|October 23, 1995
Hemangioma, supraumbilical midline raphé, and coarctation of the aorta with a right aortic arch: single causal entity?P Kishnani, A K Iafolla, A McConkie-Rosell, et al.
American Journal of Medical Genetics|September 11, 1992
Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literatureJ L Van Hove, A McConkie-Rosell, Y T Chen, et al.
Pageof 2