[Hereditary osseous and onychoid dysplasia; demonstration of linkage factors].
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Bone Diseases↗
Biomedical subjects
U PFANDLER
Publications and source records attributed to U PFANDLER.
[Combined transmission of three different hereditary diseases in the same family (deforming juvenile osteochondrosis of the hip, hypoplasia of the femur, progressive muscular dystrophy)].
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Bone Diseases↗
[Ontogeny and heredity of caput obstipum (congenital torticollis)].
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Head↗
[A family of Sugnens in Vaud exhibiting hereditary dysplasia of bone and nails; demonstration of gene linkage].
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Bone and Bones↗
[Simple recessive form of progressive muscular dystrophy with a genealogical chart from Emmental, Switzerland].
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Humans↗
[The position of human genetics in the controversy between mendelism-morganism and lyssenkoism].
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Genetics↗
[Some mutations affecting the eyes, collected as examples in the canton of Neuchatel and the Jura Bernois (congenital aniridia, universal albinism, congenital anophthalmos, total achromatopsia, oligophrenia associated with keratoconus, with ectopy of the crystalline, with congenital cataract and with atrophy of the optic nerve)].
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Albinism↗
[Genetics of cystinosis (cystine storage disease) and its relation to cystinuria and hyperaminoaciduria].
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Amino Acid Metabolism, Inborn Errors↗