[Further case of two univitelline twins with identical oxycephaly].
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Craniosynostoses↗
Biomedical subjects
D KLEIN
Publications and source records attributed to D KLEIN.
[Familial manifestations of cranio-rachiochysis associated with other malformations].
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Congenital Abnormalities↗
[Ocular manifestations of primary disorders of lipid metabolism; patho-morphologic, genetic and clinical study].
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Eye↗
[Genetic prognosis of diabetes].
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Diabetes Mellitus↗
[Familial idiocy combined with somatic and endocrine disorders].
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Diploidy↗
[Fibrocystic disease of the pancreas].
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Cystic Fibrosis↗
[Anatomo-clinical examination of a case of infantile amaurotic idiocy (Tay-Sachs)].
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Central Nervous System↗
[Genetic and nosological study of infantile amaurotic idiocy].
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Genetic Therapy↗
[Progressive and extensive manifestations of dystrophia myotonica in a family of the Aargau].
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Humans↗
[A new genealogical pedigree of granular corneal dystrophy, Groenouw I].
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Cornea↗
[Cervico-oculo-facial dysmorphia with familial deafness: Klippel-Feil, retractio bulbi, craniofacial asymetry and other congenital anomalies].
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Congenital Abnormalities↗
[Heredity of infantile amaurotic idiocy].
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Heredity↗
[Report of a case: an Alsatian family with ectodermal dysplasia].
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Ectodermal Dysplasia↗
[Dyssynergia cerebellaris myoclonica progressiva (Ramsay-Hunt) of predominant heredity in a Bern family].
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Cerebellar Diseases↗
[Studies on markers of chromosomes in a family affected with pigmentary retinitis].
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Chromosomes↗
[A new variety of Bardet-Biedl syndrome: external ophthalmoplegia, polydactylia, adiposogenital dystrophy, mental debility and hypoplasia of the hypothenar eminences].
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Bardet-Biedl Syndrome↗
[Familial hydrocephalus with concordant manifestation in univitelline twins].
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Disease↗
[Ninth International Congress on Genetics, Belagio, 24-31 August 1953 and First International Symposium on Medical Genetics, Rome, 6-7 September 1953].
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Genetics↗