Search research articles
Contact Us
Filters
Showing results (21-30 of 103) with videos related to
Page
of 11
Sort By:
Israel Journal of Medical Sciences
|
January 1, 1989
Prenatal ultrasonic diagnosis of cystic hygroma associated with fetal hydrops--report of two cases
I Meizner, M Katz, R Carmi, et al.
European Journal of Ophthalmology
|
January 1, 1997
Synthetic patch for scleral tissue loss
D 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 disease
E 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 review
D Landau, J Mordechai, M Karplus, et al.
American Journal of Medical Genetics
|
September 1, 1985
A de novo translocation, 14q21q, with a microchromosome-14p21p
D Abeliovich, M Katz, M Karplus, et al.
Prenatal Diagnosis
|
October 1, 1994
Prenatal diagnosis of Bartter syndrome
H Shalev, M Ohaly, I Meizner, et al.
American Journal of Obstetrics and Gynecology
|
July 1, 1990
Niemann-Pick disease associated with nonimmune hydrops fetalis
I Meizner, A Levy, R Carmi, et al.
American Journal of Medical Genetics
|
March 1, 1989
Duplication of distal 22q
D 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 report
I Meizner, R Carmi, M Katz, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 103) with videos related to
Sort By:
Page
of 11
Israel Journal of Medical Sciences
|
January 1, 1989
Prenatal ultrasonic diagnosis of cystic hygroma associated with fetal hydrops--report of two cases
I Meizner, M Katz, R Carmi, et al.
European Journal of Ophthalmology
|
January 1, 1997
Synthetic patch for scleral tissue loss
D 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 disease
E 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 review
D Landau, J Mordechai, M Karplus, et al.
American Journal of Medical Genetics
|
September 1, 1985
A de novo translocation, 14q21q, with a microchromosome-14p21p
D Abeliovich, M Katz, M Karplus, et al.
Prenatal Diagnosis
|
October 1, 1994
Prenatal diagnosis of Bartter syndrome
H Shalev, M Ohaly, I Meizner, et al.
American Journal of Obstetrics and Gynecology
|
July 1, 1990
Niemann-Pick disease associated with nonimmune hydrops fetalis
I Meizner, A Levy, R Carmi, et al.
American Journal of Medical Genetics
|
March 1, 1989
Duplication of distal 22q
D 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 report
I Meizner, R Carmi, M Katz, et al.
Page
of 11