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R Carmi

Showing results (21-30 of 103) with videos related to

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Israel Journal of Medical Sciences|January 1, 1989
Prenatal ultrasonic diagnosis of cystic hygroma associated with fetal hydrops--report of two casesI Meizner, M Katz, R Carmi, et al.
European Journal of Ophthalmology|January 1, 1997
Synthetic patch for scleral tissue lossD Dori, I Beiran, R Carmi, et al.
Prenatal Diagnosis|September 1, 1996
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)R Parvari, E Hershkovitz, R Carmi, et al.
American Journal of Medical Genetics|July 23, 1998
Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: histopathological delineation of an autosomal recessive diseaseE Maman, E Maor, L Kachko, et al.
American Journal of Medical Genetics|August 22, 1997
Inheritance of familial congenital isolated anorectal malformations: case report and reviewD Landau, J Mordechai, M Karplus, et al.
American Journal of Medical Genetics|September 1, 1985
A de novo translocation, 14q21q, with a microchromosome-14p21pD Abeliovich, M Katz, M Karplus, et al.
Prenatal Diagnosis|October 1, 1994
Prenatal diagnosis of Bartter syndromeH Shalev, M Ohaly, I Meizner, et al.
American Journal of Obstetrics and Gynecology|July 1, 1990
Niemann-Pick disease associated with nonimmune hydrops fetalisI Meizner, A Levy, R Carmi, et al.
American Journal of Medical Genetics|March 1, 1989
Duplication of distal 22qD Abeliovich, E Maor, N Bashan, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1989
In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case reportI Meizner, R Carmi, M Katz, et al.
Pageof 11

Showing results (21-30 of 103) with videos related to

Sort By:
Pageof 11
Israel Journal of Medical Sciences|January 1, 1989
Prenatal ultrasonic diagnosis of cystic hygroma associated with fetal hydrops--report of two casesI Meizner, M Katz, R Carmi, et al.
European Journal of Ophthalmology|January 1, 1997
Synthetic patch for scleral tissue lossD Dori, I Beiran, R Carmi, et al.
Prenatal Diagnosis|September 1, 1996
Prenatal diagnosis of glycogen storage disease type 1a by single stranded conformation polymorphism (SSCP)R Parvari, E Hershkovitz, R Carmi, et al.
American Journal of Medical Genetics|July 23, 1998
Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: histopathological delineation of an autosomal recessive diseaseE Maman, E Maor, L Kachko, et al.
American Journal of Medical Genetics|August 22, 1997
Inheritance of familial congenital isolated anorectal malformations: case report and reviewD Landau, J Mordechai, M Karplus, et al.
American Journal of Medical Genetics|September 1, 1985
A de novo translocation, 14q21q, with a microchromosome-14p21pD Abeliovich, M Katz, M Karplus, et al.
Prenatal Diagnosis|October 1, 1994
Prenatal diagnosis of Bartter syndromeH Shalev, M Ohaly, I Meizner, et al.
American Journal of Obstetrics and Gynecology|July 1, 1990
Niemann-Pick disease associated with nonimmune hydrops fetalisI Meizner, A Levy, R Carmi, et al.
American Journal of Medical Genetics|March 1, 1989
Duplication of distal 22qD Abeliovich, E Maor, N Bashan, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1989
In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case reportI Meizner, R Carmi, M Katz, et al.
Pageof 11