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E W Lovrien

Showing results (1-10 of 55) with videos related to

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Pediatric Clinics of North America|November 1, 1970
Genetic diagnosis in the newborn. A part of preventive medicineF Hecht, E W Lovrien
Journal of Pediatric Orthopedics|May 1, 1992
Diffuse capillary hemangiomas associated with skeletal hypotrophyR K Beals, E W Lovrien
Pediatrics|September 1, 1982
Management of fractures in hemophiliaL J Wolff, E W Lovrien
The Journal of Pediatrics|December 1, 1978
Chorioangioma of the placenta and intrauterine growth failureC R King, E W Lovrien
Annals of Human Genetics|July 1, 1971
Haemopexin in human serum: a search for genetic polymorphosmR 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 literatureR K Beals, E W Lovrien
Clinical Genetics|January 1, 1982
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parentsL 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 telangiectasiaC 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 manR E Magenis, F Hecht, E W Lovrien
Annales De Genetique|September 1, 1971
A mother with Down's syndrome and her chromosomally normal infantJ A Reiss, E W Lovrien, F Hecht
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Pediatric Clinics of North America|November 1, 1970
Genetic diagnosis in the newborn. A part of preventive medicineF Hecht, E W Lovrien
Journal of Pediatric Orthopedics|May 1, 1992
Diffuse capillary hemangiomas associated with skeletal hypotrophyR K Beals, E W Lovrien
Pediatrics|September 1, 1982
Management of fractures in hemophiliaL J Wolff, E W Lovrien
The Journal of Pediatrics|December 1, 1978
Chorioangioma of the placenta and intrauterine growth failureC R King, E W Lovrien
Annals of Human Genetics|July 1, 1971
Haemopexin in human serum: a search for genetic polymorphosmR 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 literatureR K Beals, E W Lovrien
Clinical Genetics|January 1, 1982
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parentsL 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 telangiectasiaC 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 manR E Magenis, F Hecht, E W Lovrien
Annales De Genetique|September 1, 1971
A mother with Down's syndrome and her chromosomally normal infantJ A Reiss, E W Lovrien, F Hecht
Pageof 6