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Clinical Pediatrics
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November 1, 1993
Status epilepticus encephalopathy with cat-scratch disease
A Ashkenasi, J Amir, H A Cohen, et al.
American Journal of Medical Genetics
|
August 22, 1997
MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome
M Frydman, M Katz, S G Cabot, et al.
The Journal of Family Practice
|
January 1, 1994
Swimming and grommets
H A Cohen, A Kauschansky, A Ashkenasi, et al.
Haematologica
|
May 1, 1984
Decreased platelet aggregation, Ca2+ and Mg2+ ATPase and platelet factor 3 activities in patients with Wilson disease
A M Cohen, H Brettbart, D Creter, et al.
American Journal of Diseases of Children (1960)
|
August 1, 1992
Mumps-associated acute cerebellar ataxia
H A Cohen, A Ashkenazi, M Nussinovitch, et al.
American Journal of Medical Genetics
|
December 23, 1999
Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)
A Aviram-Goldring, M Daniely, M Frydman, et al.
American Journal of Medical Genetics
|
December 2, 1996
t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring
D Abeliovich, J Dagan, I Lerer, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 12, 2000
Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor
M Frydman, S Vreugde, B I Nageris, et al.
American Journal of Medical Genetics
|
May 19, 2000
Noonan syndrome: a cryptic condition in early gestation
R Achiron, J Heggesh, D Grisaru, et al.
Scandinavian Journal of Gastroenterology
|
October 1, 1983
The personality pattern of patients with chronic peptic ulcer. A case-control study
J H McIntosh, R W Nasiry, M Frydman, et al.
Page
of 18
Search research articles
Search
Showing results (91-100 of 172) with videos related to
Sort By:
Page
of 18
Clinical Pediatrics
|
November 1, 1993
Status epilepticus encephalopathy with cat-scratch disease
A Ashkenasi, J Amir, H A Cohen, et al.
American Journal of Medical Genetics
|
August 22, 1997
MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome
M Frydman, M Katz, S G Cabot, et al.
The Journal of Family Practice
|
January 1, 1994
Swimming and grommets
H A Cohen, A Kauschansky, A Ashkenasi, et al.
Haematologica
|
May 1, 1984
Decreased platelet aggregation, Ca2+ and Mg2+ ATPase and platelet factor 3 activities in patients with Wilson disease
A M Cohen, H Brettbart, D Creter, et al.
American Journal of Diseases of Children (1960)
|
August 1, 1992
Mumps-associated acute cerebellar ataxia
H A Cohen, A Ashkenazi, M Nussinovitch, et al.
American Journal of Medical Genetics
|
December 23, 1999
Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)
A Aviram-Goldring, M Daniely, M Frydman, et al.
American Journal of Medical Genetics
|
December 2, 1996
t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring
D Abeliovich, J Dagan, I Lerer, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 12, 2000
Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor
M Frydman, S Vreugde, B I Nageris, et al.
American Journal of Medical Genetics
|
May 19, 2000
Noonan syndrome: a cryptic condition in early gestation
R Achiron, J Heggesh, D Grisaru, et al.
Scandinavian Journal of Gastroenterology
|
October 1, 1983
The personality pattern of patients with chronic peptic ulcer. A case-control study
J H McIntosh, R W Nasiry, M Frydman, et al.
Page
of 18