[Hereditary myatrophical ataxia--syndrome or diagnosis? Critical remarks on the nosology of hereditary degenerative diseases from the viewpoint of medical genetics].
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Ataxia↗
Biomedical subjects
B Wittwer
Publications and source records attributed to B Wittwer.
[Genetic questions in Albright's and in Jaffé-Lichtenstein syndrome].
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Endocrine System Diseases↗
[Reproductive age and population genetics--a trend analysis].
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Adolescent↗
[Use of the Y chromosome in cell nucleus morphological sex determination. Optic fluorescence methods].
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Female↗
[Testicular feminization in one of two genetic male twins].
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Androgen-Insensitivity Syndrome↗
[Clinical-genetic aspects in malformation example of microties].
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Adult↗
Dermatoglyphics and leukaemia.
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Dermatoglyphics↗
[New findings in the genetics of endogenous eczema].
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Chromosome Aberrations↗
[A clinical-genetic and dermatoglyphic contribution to the nosology of the orofaciodigital syndrome].
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Adult↗
[More precise differential diagnosis of deformities of the extremities with the use of the dermatoglyphic method].
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Dermatoglyphics↗
[Human genetic problems of malformations].
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Bone and Bones↗
[Methodical features on the genesis and nosology of craniofacial dysplasias with special consideration of cleft lip, cleft jaw, and cleft palate].
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Cleft Lip↗
[System of skin furrows and ridges in abnormalities of the extremities-genetic aspects of the phenotypic realization of blastemic disorders].
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Dermatoglyphics↗
[Situs inversus totalis-results of a clinical and dermatoglyphical examination].
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Child↗