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Lancet (London, England)
|
September 13, 1975
Letter: Elevated amniotic-fluid alpha-fetoprotein and duodenal atresia
A G Weinberg, A Milunsky, M J Harrod
Southern Medical Journal
|
December 1, 1980
Childhood allergy
S R Halpern, G W Brasher, M J Harrod
American Journal of Human Genetics
|
March 1, 1974
Homozygous familial hypercholesterolemia: specificity of the biochemical defect in cultured cells and feasibility of prenatal detection
J L Goldstein, M J Harrod, M S Brown
Humangenetik
|
July 23, 1975
Ring 17 chromosome detected by amniocentesis
A G Weinberg, J L Bair, M J Harrod
American Journal of Medical Genetics
|
September 1, 1992
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment
J M Friedman, M J Harrod, P N Howard-Peebles
Clinical Genetics
|
February 1, 1976
Polycystic kidney disease in a patient with the oral-facial-digital syndrome - type I
M J Harrod, J Stokes, L F Peede, et al.
American Journal of Medical Genetics
|
January 1, 1980
Duplication 12q mosaicism in two unrelated patients with a similar syndrome
M J Harrod, J B Byrne, V G Dev, et al.
Journal of the American Academy of Dermatology
|
November 1, 1993
Methotrexate and reproduction in men: case report and recommendations
L F Morris, M J Harrod, M A Menter, et al.
The Journal of Urology
|
December 1, 1981
Familial absorptive hypercalciuria in a large kindred
C Y Pak, J McGuire, R Peterson, et al.
American Journal of Obstetrics and Gynecology
|
September 1, 1984
Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound
M J Harrod, J M Friedman, R Santos-Ramos, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Lancet (London, England)
|
September 13, 1975
Letter: Elevated amniotic-fluid alpha-fetoprotein and duodenal atresia
A G Weinberg, A Milunsky, M J Harrod
Southern Medical Journal
|
December 1, 1980
Childhood allergy
S R Halpern, G W Brasher, M J Harrod
American Journal of Human Genetics
|
March 1, 1974
Homozygous familial hypercholesterolemia: specificity of the biochemical defect in cultured cells and feasibility of prenatal detection
J L Goldstein, M J Harrod, M S Brown
Humangenetik
|
July 23, 1975
Ring 17 chromosome detected by amniocentesis
A G Weinberg, J L Bair, M J Harrod
American Journal of Medical Genetics
|
September 1, 1992
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment
J M Friedman, M J Harrod, P N Howard-Peebles
Clinical Genetics
|
February 1, 1976
Polycystic kidney disease in a patient with the oral-facial-digital syndrome - type I
M J Harrod, J Stokes, L F Peede, et al.
American Journal of Medical Genetics
|
January 1, 1980
Duplication 12q mosaicism in two unrelated patients with a similar syndrome
M J Harrod, J B Byrne, V G Dev, et al.
Journal of the American Academy of Dermatology
|
November 1, 1993
Methotrexate and reproduction in men: case report and recommendations
L F Morris, M J Harrod, M A Menter, et al.
The Journal of Urology
|
December 1, 1981
Familial absorptive hypercalciuria in a large kindred
C Y Pak, J McGuire, R Peterson, et al.
American Journal of Obstetrics and Gynecology
|
September 1, 1984
Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound
M J Harrod, J M Friedman, R Santos-Ramos, et al.
Page
of 4