MEDICAL GENETICS 1962
No abstract listed.
Familial true hermaphrodism in pre- and postpuberal genetic females; hormonal and morphologic studies
Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia
The temporal bone in osteogenesis imperfecta congenita. A contribution to the question of the etiology of otosclerosis
Histidinemia. A deficiency in histidase resulting in the urinary excretion of histidine and of imidazolepyruvic acid
Arteriovenous pulmonary aneurysms in Osler's disease (telangiectasia hereditaria haemorrhagica). Report of four cases in the same family
Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family
A rapid screening dye test for the detection of glucose-6-phosphate dehydrogenase deficiency in red cells
An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder
Persistence of mucopolysaccharide inclusions in cultures of lymphocytes from patients with gargoylism
Blood Clotting Disorders
Thrombophilia includes conditions with increased tendency for excessive blood clotting. Blood clotting occurs when the body has insufficient amounts of specialized proteins that make blood clot and stop bleeding. Here is the latest research on blood clotting disorders.