Penrose, Lionel Sharples
Penrose, Lionel Sharples 1896-1972
Penrose, L. S. (Lionel Sharples)
Penrose, Lionel Sharples, 1898-1972
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Penrose, L.S. (Lionel Sharples), 1898-1972
Lionel Penrose British psychiatrist, medical geneticist, mathematician, and chess theorist (*1898 – †1972)
Penrose, L.S.
Penrose, Lionel S. 1898-1972
VIAF ID: 55247667 (Personal)
Permalink: http://viaf.org/viaf/55247667
Preferred Forms
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100 1 _ ‡a Penrose, L. S. ‡q (Lionel Sharples)
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100 1 _ ‡a Penrose, L. S. ‡q (Lionel Sharples)
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100 1 _ ‡a Penrose, L. S. ‡q (Lionel Sharples), ‡d 1898-1972
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100 1 _ ‡a Penrose, L.S.
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100 1 _ ‡a Penrose, L.S. ‡q (Lionel Sharples), ‡d 1898-1972
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100 1 _ ‡a Penrose, Lionel Sharples
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100 1 _ ‡a Penrose, Lionel Sharples
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100 1 _ ‡a Penrose, Lionel Sharples ‡d (1896-1972)
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100 1 _ ‡a Penrose, Lionel Sharples ‡d (1896-1972).
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4xx's: Alternate Name Forms (23)
5xx's: Related Names (3)
- 551 _ _
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London
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ortg
‡4
https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 551 _ _
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London
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orts
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https://d-nb.info/standards/elementset/gnd#placeOfDeath
- 500 1 _
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Penrose, Roger
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1931-
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bezf
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https://d-nb.info/standards/elementset/gnd#familialRelationship
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Beziehung familiaer
Works
| Title | Sources |
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| “Ability and opportunity in english education.”. |
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| The biology of mental defect |
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| Birth weight and gestation time in relation to maternal age, parity and infant survival |
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| The blood group distribution in the eastern counties of England |
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| The blood grouping of mongolian imbeciles. |
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| The causes of blindness in chilhood : a study of 776 children with severe visual handicaps |
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| The complex determinants of amentia. |
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| The creases on the minimal digit in mongolism |
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| Crystalline bodies in lymphocytes of patients with Down's syndrome |
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| Dermatoglyphic patterns in a case of trisomy 8. |
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| The detection of autosomal linkage in data which consist of pairs of brothers and sisters of unspecified parentage |
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| Down's anomaly |
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| Einführung in die Humangenetik |
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| The Elementary Statistics of Majority Voting |
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| Evolucija : klasici i suvremene spoznaje |
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| Finger-print pattern and the sex chromosomes |
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| Fingerprints and palmistry |
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| Genetic linkage in graded human characters |
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| Genetic studies of genius. Vol. III, the promise of youth |
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| The genetics of dermal ridges |
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| Hautleistenbefunde in der Medizin |
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| A homozygous chromosomal variant. |
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| Human chromosomes, normal and aberrant |
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| Intestinal polyposis |
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| Introduction à la génétique humaine |
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| Kennedy-Galton Centre, Harperbury Hospital |
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| Mathematical tables for research workers in human genetics |
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| Memorandum on dermatoglyphic nomenclature |
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| Mental disease and crime : outline of a comparative study of European statistics |
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| Mental Retardation |
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| Mentally handicapped children : a handbook for parents |
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| MICROCEPHALY |
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| Mongolism and Duration of Marriage |
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| Note on dermatoglyphic data in a brachydactylous family |
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| Notes on the interpretation of intrafamilialcorrelation coefficients |
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| On the geometry of loops and deltas |
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| On the interaction of heredity and environment in the study of human genetics (with special reference to mongolian imbecility) |
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| On the objective study of crowd behaviour |
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| Outline of human genetics |
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| The over-the-board chess match, London, September, 1947 : Great Britain v. U.S.S.R. |
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| Pedigrees of hereditary diseases and abnormalities found in the Japanese race |
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| Primary and Secondary Amentia |
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| Proceedings of the third congress of the International Association for the Scientific Study of Mental Deficiency, the Hague, the Netherlands, 4th-12th September 1973 ... |
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| Psychiatrie sociale : Génétique et eugénique |
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| The relative effects of paternal and maternal age in mongolism. 1933. |
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| Seishin hakujaku no igaku |
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| Survey of cases of familial mental illness. L. S. Penrose, July 1945. |
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| The treasury of human inheritance. |
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| Two Cases of Phenylpyruvic Amentia |
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| De wereld van Nigel Hunt : het dagboek van een mongoloïde jongen |
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| Wstęp do genetyki człowieka / L. S. Penrose. - Warszawa, 1965. |
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| 精神薄弱の医学 |
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