[Recessive deaf-mutism in Werdenberg (Saint Gallen canton, Switzerland)].
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Deafness↗
Biomedical subjects
U PFANDLER
Publications and source records attributed to U PFANDLER.
[Speech disorders from the viewpoint of the geneticist].
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Humans↗
[Recessive deaf-mutism in Werdenberg (St. Gallen)].
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Biometry↗
[Hereditary metabolic disorders].
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Metabolic Diseases↗
[Lethal factors in humans].
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Antigens, Bacterial↗
[Heterozygotic and homozygotic manifestation of certain metabolic disorders: chronic porphyria, cystinosis, Niemann-Pick disease].
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Cystinosis↗
[Semilethal form of recessive deaf-mutism].
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Deafness↗
[The contribution of biochemistry to the development of human pheno-genetics].
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Biochemical Phenomena↗
The heterozygous and homozygous manifestation of certain metabolic disorders; chronic porphyria, cystinosis, Niemann-Pick disease.
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Cystine↗
[Genetic prognosis for irregularly dominant heredity].
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Genetics↗
[Severe ariboflavinosis, late rickets and amino diabetes with chronic hereditary coproporphyria].
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Coproporphyria, Hereditary↗
[Hereditary mechanism of Dupuytren's disease].
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Dupuytren Contracture↗
[The hereditary mechanism of multiple cartilaginous exostosis].
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Enchondromatosis↗
[A pair of bivitelline twins having Friedreich's ataxia in a family with simple recessive heredity with double consanguinity].
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Consanguinity↗
[Results of parents' ignoring genetic counseling].
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Congenital Abnormalities↗
[New concepts on heredity and pathogenesis of the Niemann-Pick disease].
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Heredity↗
[Bilateral hereditary dysplasia of the hips and knees in a family of the Swiss Urals].
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Disease↗
[Development in genetics; from micromerism to the biological atomic theory].
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Genetics↗