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Pediatric Clinics of North America
|
November 1, 1970
Genetic diagnosis in the newborn. A part of preventive medicine
F Hecht, E W Lovrien
Journal of Pediatric Orthopedics
|
May 1, 1992
Diffuse capillary hemangiomas associated with skeletal hypotrophy
R K Beals, E W Lovrien
Pediatrics
|
September 1, 1982
Management of fractures in hemophilia
L J Wolff, E W Lovrien
The Journal of Pediatrics
|
December 1, 1978
Chorioangioma of the placenta and intrauterine growth failure
C R King, E W Lovrien
Annals of Human Genetics
|
July 1, 1971
Haemopexin in human serum: a search for genetic polymorphosm
R E Stewart, E W Lovrien
Clinical Orthopaedics and Related Research
|
May 1, 1976
Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature
R K Beals, E W Lovrien
Clinical Genetics
|
January 1, 1982
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents
L Bufton, R E Magenis, E W Lovrien
Clinical Genetics
|
December 1, 1977
Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia
C R King, E W Lovrien, J Reiss
Science (New York, N.Y.)
|
October 2, 1970
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man
R E Magenis, F Hecht, E W Lovrien
Annales De Genetique
|
September 1, 1971
A mother with Down's syndrome and her chromosomally normal infant
J A Reiss, E W Lovrien, F Hecht
Page
of 6
Search research articles
Search
Showing results (1-10 of 55) with videos related to
Sort By:
Page
of 6
Pediatric Clinics of North America
|
November 1, 1970
Genetic diagnosis in the newborn. A part of preventive medicine
F Hecht, E W Lovrien
Journal of Pediatric Orthopedics
|
May 1, 1992
Diffuse capillary hemangiomas associated with skeletal hypotrophy
R K Beals, E W Lovrien
Pediatrics
|
September 1, 1982
Management of fractures in hemophilia
L J Wolff, E W Lovrien
The Journal of Pediatrics
|
December 1, 1978
Chorioangioma of the placenta and intrauterine growth failure
C R King, E W Lovrien
Annals of Human Genetics
|
July 1, 1971
Haemopexin in human serum: a search for genetic polymorphosm
R E Stewart, E W Lovrien
Clinical Orthopaedics and Related Research
|
May 1, 1976
Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature
R K Beals, E W Lovrien
Clinical Genetics
|
January 1, 1982
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents
L Bufton, R E Magenis, E W Lovrien
Clinical Genetics
|
December 1, 1977
Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia
C R King, E W Lovrien, J Reiss
Science (New York, N.Y.)
|
October 2, 1970
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man
R E Magenis, F Hecht, E W Lovrien
Annales De Genetique
|
September 1, 1971
A mother with Down's syndrome and her chromosomally normal infant
J A Reiss, E W Lovrien, F Hecht
Page
of 6