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Familial Cancer
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October 24, 2003
Familial adenomatous polyposis at the Tel Aviv Medical Center: demographic and clinical features
P Rozen, Z Samuel, M Rabau, et al.
Gastroenterology
|
December 31, 1998
Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer
P Rozen, R Shomrat, H Strul, et al.
Fetal Diagnosis and Therapy
|
February 25, 1998
Doppler velocimetry of the umbilical artery as a predictor of outcome in pregnancies characterized by elevated beta-subunit human chorionic gonadotropin
Y Yaron, A J Jaffa, J Har-Toov, et al.
Prenatal Diagnosis
|
August 1, 1996
Second-trimester maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated oestriol after early transvaginal multifetal pregnancy reduction
A Groutz, A Amit, Y Yaron, et al.
Human Mutation
|
June 1, 2001
Novel mutations in the emerin gene in Israeli families
Y Nevo, S Ahituv, Y Yaron, et al.
Prenatal Diagnosis
|
September 1, 1989
Prenatal diagnosis of Lesch-Nyhan syndrome: experience with three fetuses at risk
E Zoref-Shani, Y Bromberg, B Goldman, et al.
Archives of Pathology & Laboratory Medicine
|
March 1, 1980
Ultrastructure of the conjunctiva, skin, and gingiva: a case of Sandhoff's disease in a Jewish patient
G Messer, S Harel, B Erlich, et al.
American Journal of Medical Genetics
|
February 5, 1998
SMA type 2 unrelated to chromosome 5q13
Y Nevo, U Kramer, C Legum, et al.
Israel Journal of Medical Sciences
|
October 1, 1975
Acute neonatal isovaleric acidemia. A report of two cases
Z Spirer, S Swirsky-Fein, V Zakut, et al.
AJR. American Journal of Roentgenology
|
January 1, 1977
The Dyggve-Melchio-Clausen syndrome
S Schorr, C Legum, M Ochshorn, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 6
Familial Cancer
|
October 24, 2003
Familial adenomatous polyposis at the Tel Aviv Medical Center: demographic and clinical features
P Rozen, Z Samuel, M Rabau, et al.
Gastroenterology
|
December 31, 1998
Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer
P Rozen, R Shomrat, H Strul, et al.
Fetal Diagnosis and Therapy
|
February 25, 1998
Doppler velocimetry of the umbilical artery as a predictor of outcome in pregnancies characterized by elevated beta-subunit human chorionic gonadotropin
Y Yaron, A J Jaffa, J Har-Toov, et al.
Prenatal Diagnosis
|
August 1, 1996
Second-trimester maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated oestriol after early transvaginal multifetal pregnancy reduction
A Groutz, A Amit, Y Yaron, et al.
Human Mutation
|
June 1, 2001
Novel mutations in the emerin gene in Israeli families
Y Nevo, S Ahituv, Y Yaron, et al.
Prenatal Diagnosis
|
September 1, 1989
Prenatal diagnosis of Lesch-Nyhan syndrome: experience with three fetuses at risk
E Zoref-Shani, Y Bromberg, B Goldman, et al.
Archives of Pathology & Laboratory Medicine
|
March 1, 1980
Ultrastructure of the conjunctiva, skin, and gingiva: a case of Sandhoff's disease in a Jewish patient
G Messer, S Harel, B Erlich, et al.
American Journal of Medical Genetics
|
February 5, 1998
SMA type 2 unrelated to chromosome 5q13
Y Nevo, U Kramer, C Legum, et al.
Israel Journal of Medical Sciences
|
October 1, 1975
Acute neonatal isovaleric acidemia. A report of two cases
Z Spirer, S Swirsky-Fein, V Zakut, et al.
AJR. American Journal of Roentgenology
|
January 1, 1977
The Dyggve-Melchio-Clausen syndrome
S Schorr, C Legum, M Ochshorn, et al.
Page
of 6