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Brain & Development
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January 1, 1990
Mucolipidosis III and Bardet-Biedl syndrome in the same family: diagnostic pitfalls
C R Gordon, Y Bar-Ziv, M Frydman, et al.
The Australian and New Zealand Journal of Surgery
|
February 1, 1997
The practice of carotid endarterectomy in Australasia
G M Frydman, C A Codd, D M Cavaye, et al.
American Journal of Medical Genetics
|
July 1, 1991
Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome
M Frydman, A L Weinstock, H A Cohen, et al.
American Journal of Medical Genetics
|
September 11, 1995
Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family
M Frydman, R Straussberg, R Shomrat, et al.
Msystems
|
February 21, 2023
Construction and Modeling of a Coculture Microplate for Real-Time Measurement of Microbial Interactions
Charles Jo, David B Bernstein, Natalie Vaisman, et al.
American Journal of Medical Genetics
|
March 21, 1998
Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiency
A Kauschansky, M Shohat, M Frydman, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Different phenotypic expression in monozygotic twins with Huntington disease
M H Anca, E Gazit, R Loewenthal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 8, 2013
Evolutionarily conserved Wolbachia-encoded factors control pattern of stem-cell niche tropism in Drosophila ovaries and favor infection
Michelle E Toomey, Kanchana Panaram, Eva M Fast, et al.
Scandinavian Journal of Urology and Nephrology
|
January 1, 1993
Urodynamic manifestations associated with Ramsay-Hunt syndrome. Case report
H A Cohen, J Abarbanel, A Ashkenasi, et al.
The Journal of Family Practice
|
January 1, 1994
Swimming and grommets
H A Cohen, A Kauschansky, A Ashkenasi, et al.
Page
of 18
Search research articles
Search
Showing results (81-90 of 172) with videos related to
Sort By:
Page
of 18
Brain & Development
|
January 1, 1990
Mucolipidosis III and Bardet-Biedl syndrome in the same family: diagnostic pitfalls
C R Gordon, Y Bar-Ziv, M Frydman, et al.
The Australian and New Zealand Journal of Surgery
|
February 1, 1997
The practice of carotid endarterectomy in Australasia
G M Frydman, C A Codd, D M Cavaye, et al.
American Journal of Medical Genetics
|
July 1, 1991
Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome
M Frydman, A L Weinstock, H A Cohen, et al.
American Journal of Medical Genetics
|
September 11, 1995
Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family
M Frydman, R Straussberg, R Shomrat, et al.
Msystems
|
February 21, 2023
Construction and Modeling of a Coculture Microplate for Real-Time Measurement of Microbial Interactions
Charles Jo, David B Bernstein, Natalie Vaisman, et al.
American Journal of Medical Genetics
|
March 21, 1998
Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiency
A Kauschansky, M Shohat, M Frydman, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2003
Different phenotypic expression in monozygotic twins with Huntington disease
M H Anca, E Gazit, R Loewenthal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 8, 2013
Evolutionarily conserved Wolbachia-encoded factors control pattern of stem-cell niche tropism in Drosophila ovaries and favor infection
Michelle E Toomey, Kanchana Panaram, Eva M Fast, et al.
Scandinavian Journal of Urology and Nephrology
|
January 1, 1993
Urodynamic manifestations associated with Ramsay-Hunt syndrome. Case report
H A Cohen, J Abarbanel, A Ashkenasi, et al.
The Journal of Family Practice
|
January 1, 1994
Swimming and grommets
H A Cohen, A Kauschansky, A Ashkenasi, et al.
Page
of 18