DELETION ON SHORT ARMS OF A B-CHROMOSOME WITHOUT "CRI DU CHAT" SYNDROME.
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Chromosome Aberrations↗
Biomedical subjects
H REINWEIN
Publications and source records attributed to H REINWEIN.
[DETECTION AND INTERPRETATION OF SYMPTOMS. I].
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Diagnosis, Differential↗
[FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME].
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Chromosome Aberrations↗
[On the clinical aspects of embolic and thrombotic occlusion of the renal artery].
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Emaciation↗
[On the incidence, course and therapy of rheumatic carditis in children].
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Child↗
[On the clinical aspects and epidemiology of psittacosis and ornithosis].
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Humans↗
[Advances in the diagnosis and therapy of diabetic coma].
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Diabetic Coma↗
[Diagnosis and therapy of sporadic cretinism].
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Congenital Hypothyroidism↗
[Studies on the problem of human milk-adapted infant nutrition].
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Animals↗
[Asbestosis in insulation workers].
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Asbestosis↗
[Recognition and significance of malabsorption syndrome].
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Celiac Disease↗
[Clinical aspects of gout, the so-called forgotten disease].
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Gout↗
Congenitals complete the AV block.
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Cardiovascular Diseases↗
[Demonstration of vasopressor substances in urine].
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Body Fluids↗
[The post-cholecystectomy syndrome].
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Cholecystectomy↗
[Familial incidence of so-called Ullrich-Turner syndrome and the existence of a pterygium colli, a cryptorchidism and of Meig's syndrome in two brothers with congenital anomalies].
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Cryptorchidism↗
[A year-long therapy resistant hypochromic anemia of unexplained etiology].
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Anemia↗