Tooth transplantation in the mouse. I. The use of procion dyes and tritiated proline in a study of syngeneic tooth germ transplantation.
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Animals↗
Biomedical subjects
D Klein
Publications and source records attributed to D Klein.
A balanced 13-18 translocation [46,XY,t(13q-;18q+)] in the father of an infant with multiple anomalies.
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Abnormalities, Multiple↗
[The frequency and distribution of satellites in a group with chromosomal anomalies as compared with a group of normal individuals].
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Adult↗
Genetic approach to the nosology of retinal disorders.
During the last 20 years we have carried out, with the collaborators of our Institute, a series of genetic and epidemiologic investigations on tapetoretinal degenerations and allied diseases in Switzerland. Basing conclusions both on the results of this inquiry and on the findings in the literature, we give in this study a general survey of the chorioretinal abiotrophies and describe in particular their clinical and genetic aspects as well as their association with other congenital and hereditary anomalies. A nosologic classification is proposed which takes into account the clinical and genetic features of the systemic heredodegenerative conditions of the retina.
Abnormalities, Multiple↗
[Long-term psychopathological study of a recidivist delinquent presenting the XYY syndrome].
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Adult↗
[The risk of reappearance of a harelip-cleft palate or other congenital anomalies (congenital hip dislocation, cutaneous syndactyly) in a family].
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Abnormalities, Multiple↗
[Genetic aspects of sexual deviations. The study of monozygotic twins, deaf-mutes, showing discordance in psychosexual behavior].
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Adult↗
A malignant form of neurogenic muscular atrophy in adults, with dominant inheritance.
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Adult↗
[Genetic aspects of mental retardation].
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Humans↗
Rapid evaluation of maxillofacial injuries.
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Hemorrhage↗
H-2 types of translocation stocks T(2;9)138Ca, T(9;13)-190Ca and an H-2 recombinant.
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Alleles↗
Persistence of H-2 and some non-H-2 antigens on long-term-cultured mouse cell lines.
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Animals↗
[Mandibulofacial dysostosis (Franceschetti's syndrome of complete form) in a 15-month-old].
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Ear, External↗
[An atypical form of spondyle-epiphyseal dysostosis (pseudo-Morquio)].
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Child, Preschool↗
[An extensive form of mandibulo-facial dysostosis (Franceschetti) with malformations of the extremities and other congenital anomalies in a girl whose brother presents only an incomplete form of the syndrome (fistula auris congenita retrotragica)].
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Abnormalities, Multiple↗
[Segregation analysis of myotonia atrophica].
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Age Factors↗
[A genetic questionnaire. The genetic aspects of a case of benign spinal muscular dystrophy].
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Age Factors↗