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Human Heredity|January 1, 1977
Congenital hypomegakaryocytic thrombocytopenia associated with bilateral absence of the radius - the TAR syndromeS B Edelberg, J Cohn, N J BrandtJournal of Inherited Metabolic Disease|January 1, 1984
Symptoms and signs in organic aciduriasN J BrandtJournal of Inherited Metabolic Disease|January 1, 1978
Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locusE Christensen, N J BrandtClinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduriaE Christensen, N J BrandtPrenatal Diagnosis|March 1, 1985
Disaccharidase deficiency in amniotic fluid from cases of cystic fibrosisM Schwartz, N J BrandtArchives of Disease in Childhood|February 1, 1981
Congenital hypothyroidism in DenmarkB B Jacobsen, N J BrandtTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 6, 2002
[Torture survivors in Norway--physician's responsibility]J CohnScandinavian Journal of Haematology|March 1, 1976
Thrombocytopenia in childhood: an evaluation of 433 patientsJ CohnMedical Education|May 1, 1996
Medical education on violations of human rights: the responsibility of health personnelJ CohnJournal of Sex & Marital Therapy|December 24, 2022
Some Limitations of "Challenges in the Care of Transgender and Gender-Diverse Youth: An Endocrinologist's View"J CohnPageof 47