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Human Genetics
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September 22, 1977
Hirschsprung's disease and congenital deafness. Familial assocation
A G Weinberg, G Currarino, A M Besserman
Pediatric Pathology
|
July 1, 1993
Thyroid C cells in the DiGeorge anomaly: a quantitative study
S Pueblitz, A G Weinberg, J Albores-Saavedra
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 11, 1991
Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome
G N Wilson, R H Squires, A G Weinberg
The Journal of Pediatrics
|
February 1, 1983
Pulmonary microthrombi syndrome in newborn infants with unresponsive persistent pulmonary hypertension
D L Levin, A G Weinberg, R M Perkin
International Journal of Cancer
|
March 10, 2001
Loss of p16(INK4a) expression correlates with decreased survival in pediatric osteosarcomas
A Maitra, H Roberts, A G Weinberg, et al.
Circulation
|
August 1, 1979
Hemodynamic, pulmonary vascular, and myocardial abnormalities secondary to pharmacologic constriction of the fetal ductus arteriosus. A possible mechanism for persistent pulmonary hypertension and transient tricuspid insufficiency in the newborn infant
D L Levin, L J Mills, A G Weinberg
The Journal of Pediatrics
|
March 1, 1976
The occurrence of hepatoma in the chronic form of hereditary tyrosinemia
A G Weinberg, C E Mize, H G Worthen
Pediatrics
|
December 31, 1997
Subcutaneous granuloma annulare: a review of 47 cases
E I Felner, J B Steinberg, A G Weinberg
Archives of Pathology & Laboratory Medicine
|
August 25, 2001
Aberrant expression of tumor suppressor proteins in the Ewing family of tumors
A Maitra, H Roberts, A G Weinberg, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 84) with videos related to
Sort By:
Page
of 9
Human Genetics
|
September 22, 1977
Hirschsprung's disease and congenital deafness. Familial assocation
A G Weinberg, G Currarino, A M Besserman
Pediatric Pathology
|
July 1, 1993
Thyroid C cells in the DiGeorge anomaly: a quantitative study
S Pueblitz, A G Weinberg, J Albores-Saavedra
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 11, 1991
Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome
G N Wilson, R H Squires, A G Weinberg
The Journal of Pediatrics
|
February 1, 1983
Pulmonary microthrombi syndrome in newborn infants with unresponsive persistent pulmonary hypertension
D L Levin, A G Weinberg, R M Perkin
International Journal of Cancer
|
March 10, 2001
Loss of p16(INK4a) expression correlates with decreased survival in pediatric osteosarcomas
A Maitra, H Roberts, A G Weinberg, et al.
Circulation
|
August 1, 1979
Hemodynamic, pulmonary vascular, and myocardial abnormalities secondary to pharmacologic constriction of the fetal ductus arteriosus. A possible mechanism for persistent pulmonary hypertension and transient tricuspid insufficiency in the newborn infant
D L Levin, L J Mills, A G Weinberg
The Journal of Pediatrics
|
March 1, 1976
The occurrence of hepatoma in the chronic form of hereditary tyrosinemia
A G Weinberg, C E Mize, H G Worthen
Pediatrics
|
December 31, 1997
Subcutaneous granuloma annulare: a review of 47 cases
E I Felner, J B Steinberg, A G Weinberg
Archives of Pathology & Laboratory Medicine
|
August 25, 2001
Aberrant expression of tumor suppressor proteins in the Ewing family of tumors
A Maitra, H Roberts, A G Weinberg, et al.
Page
of 9