Hostname: page-component-76fb5796d-dfsvx Total loading time: 0 Render date: 2024-04-29T09:22:52.982Z Has data issue: false hasContentIssue false
  • English
  • Français

Kennedy-Galton Centre, Harperbury Hospital

Published online by Cambridge University Press:  09 July 2009

L. S. Penrose
Get access Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Research Report
Information
Psychological Medicine , Volume 3 , Issue 1 , February 1973 , pp. 125 - 129
Copyright
Copyright © Cambridge University Press 1973

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

BIBLIOGRAPHY AND REFERENCES

Berg, J. M. (1968). A study of the td dermal ridge-count on the human palm. Human Biology, 40, 375–385.Google Scholar
Berg, J. M. (1968). Observations on thenar/first interdigital dermatoglyphic patterns in mongolism. Journal of Mental Deficiency Research, 12, 307–311.Google ScholarPubMed
Berg, J. M., and Bavin, J. T. R. (1969). Mongolism and maternai menarche. Journal of Medical Genetics, 6, 135–136.Google Scholar
Berg, J. M., Delhanty, J. D. A., Faunch, J. A., and Ridler, M. A. C. (1965). Partial deletion of short arm of a chromosome of the 4–5 group (Denver) in an adult male. Journal of Mental Deficiency Research, 9, 219–228.Google Scholar
Berg, J. M., Faunch, J. A., Pendrey, M. J., Penrose, L. S., Ridler, M. A. C., and Shapiro, A. (1969). A homozygous chromosomal variant. Lancet, 1, 531.Google Scholar
Berg, J. M., Gilderdale, S., and Way, J. (1969). On telling parents of a diagnosis of mongolism. British Journal of Psychiatry, 115, 1195–1196.Google Scholar
Berg, J. M., Green, E. A., and Ridler, M. A. C. (1966). Epiloia (tuberous sclerosis): a report of a case with unusual tumours. Journal of Medical Genetics, 3, 153–155.CrossRefGoogle ScholarPubMed
Berg, J. M., McCreary, B. D., Ridler, M. A. C., and Smith, G. F. (1970). The de Lange syndrome. Institute for Research into Mental Retardation Monograph No. 2. Pergamon Press: Oxford.Google Scholar
Berg, J. M., Ridler, M. A. C., and McQuaid, A. (1969). Sex chromatin survey of women in a special psychiatric hospital. Nature, 222, 896–897.CrossRefGoogle Scholar
Berg, J. M., Smith, G. F., Ridler, M. A. C., Dutton, G., Green, E. A., and Richards, B. W. (1966). On the association of broad thumbs and first toes with other physical peculiarities and mental retardation. Journal of Mental Deficiency Research, 10, 204–220.Google Scholar
Gilderdale, S. (1970). Parents under strain. New Society, No. 397, 777–778.Google Scholar
Laxová, R. (1972). Antenatal development of amylase enzymes. Journal of Medical Genetics, 9, 321–323.Google Scholar
Laxová, R., and Kamarýt, J. (1970a). Genetic aspects of human α-amylase heterogeneity. In Enzymes and Isoenzymes. Edited by D. Shugar. FEBS Symposium, 18, 335–339.Google Scholar
Laxová, R., and Kamarýt, J. (1970b). Amylase heterogeneity in patients with Down's syndrome, Journal of Mental Deficiency Research 14, 250, 253.Google Scholar
Laxová, R., McKcown, J. A., Saldaña, P., and Timothy, J. A. D. (1971). A case of XYY Down's syndrome confirmed by autoradiography. Journal of Medical Genetics, 8, 215–219.Google Scholar
Laxová, R., O'Hara, P. T., and Timothy, J. A. D. (1972). A further example of a lethal autosomal recessive condition in man. Journal of Mental Deficiency Research, 16, 139–143.Google Scholar
O'Hara, P. T. (1970). Spiral tilt of triplet fibers in human leukocyte centrioles. Journal of Ultrastructurc Research, 31, 195–198.Google Scholar
O'Hara, P. T.Electron microscopical study of the brain in Down's syndrome. Brain, 95. (In press.)Google Scholar
Penrose, L. S. (1966a). The causes of Down's syndrome. In Advances in Teratology, Vol. 1, pp. 9–24. Edited by Woollam, D. H. M.. Logos Press: London.Google Scholar
Penrose, L. S. (1966b). Dermatoglyphic patterns in large acrocentric trisomy. Journal of Mental Deficiency Research, 10, 1–18.Google Scholar
Penrose, L. S. (1966c). Heredity, environment and mental subnormality. Journal of Mental Subnormality, 12, 55–60.Google Scholar
Penrose, L. S. (1966d). The contribution of mental deficiency research to psychiatry. British Journal of Psychiatry, 112, 747–755.Google Scholar
Penrose, L. S. (1967a). Finger-print pattern and the sex chromosomes. Lancet, 1, 298–300.Google Scholar
Penrose, L. S. (1967b). The effects of change in maternal age distribution upon the incidence of mongolism. Journal of Mental Deficiency Research, 11, 54–57.Google ScholarPubMed
Penrose, L. S. (1968a). Dermatoglyphs in human polyploidy. Journal of Medical Genetics, 5, 1–3.Google Scholar
Penrose, L. S. (1968b). Memorandum on dermatoglyphic nomenclature. Birth Defects: Original Article Series, 4, no. 3.Google Scholar
Penrose, L. S. (1969a). Dermatoglyphics in trisomy 17 or 18. Journal of Mental Deficiency Research, 13, 44–59.Google Scholar
Penrose, L. S. (1969b). Effects of additive genes at many loci compared with those of a set of alleles at one locus in parent-child and sib correlations. Annals of Human Genetics, 33, 15–21.Google Scholar
Penrose, L. S. (1970). Measurement in mental deficiency. British Journal of Psychiatry, 116, 369–375.Google Scholar
Penrose, L. S. (1972). Mental ability and chromosomal errors. Proceedings of the Second Congress of the International Association for the Scientific Study of Mental Deficiency, Warsaw, 1970, pp. 79–86. Edited by Primrose, D. A. A.. Swets and Zeitlinger: Amsterdam.Google Scholar
Penrose, L. S. (1972). The maintenance of the helpless idiot. In Patient, Doclor, Society–A Symposium of Introspections, pp. 29–34. Edited by McLachlan, G.. Published for the Nuffield Provincial Hospitals Trust by the Oxford University Press: London.Google Scholar
Penrose, L. S. (1972). Biology of Mental Defect. 4th edn.Sidgwick and Jackson: London.Google Scholar
Penrose, L. S., and Berg, J. M. (1968). Mongolism and duration of marriage. Nature, 218, 300.CrossRefGoogle ScholarPubMed
Penrose, L. S., and Loesch, D. (1967). A study of dermal ridge width in the second (palmar) interdigital area with special reference to ancuploid states. Journal of Mental Deficiency Research, 11, 36–42.Google ScholarPubMed
Penrose, L. S., and Loesch, D. (1969). Dermatoglyphic sole patterns: a new attempt at classification. Human Biology, 41, 427–448.Google Scholar
Penrose, L. S., and Loesch, D. (1971). Dermatoglyphic patterns and clinical diagnosis by discriminant Function. Annals of Human Genetics. 35, 15, 60.Google Scholar
Penrose, L. S., and Loesch, D. (1972). Classification of normal and abnormal dermatoglyphics. Proceedings of the Second Congress of the International Association for the Scientific Study of Mental Deficiency, Warsaw, 1970. pp. 155–360. Edited by Primrose, D. A. A.. Swets and Zeillinger: Amsterdam.Google Scholar
Penrose, L. S., and Plomley, N. J. B. (1969). Structure of Interstitial epidermal ridges. Zeitschrift für Morphologie und Anthropologie, 61, 81–84.Google Scholar
Penrose, L. S., and Smith, G. F. (1966). Down's Anomaly. Churchill: London.Google Scholar
Ridler, M. A. C. (1971). Banding patterns of metaphase chromosomes in Down's syndrome. Lancet, 2, 603.CrossRefGoogle ScholarPubMed
Ridler, M. A. C., Berg, J. M., Pendrey, M. J., Saldaña, P., and Timothy, J. A. D. (1970). Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women. Journal of Medical Genetics, 7, 148–152.CrossRefGoogle ScholarPubMed
Ridler, M. A. C., and Faunch, J. A. (1969). Long arm measurements of chromosomes 4 and 5 with special reference to the cri du chat syndrome. Annals of Human Genetics, 32, 375–381.Google Scholar
Ridler, M. A. C., Garrod, O., and Berg, J. M. (1971). A case of Prader-Willi syndrome in a girl with a small extra chromosome. Acta Paediatrica Scandinavica, 60, 222–226.CrossRefGoogle Scholar
Ridler, M. A. C., Pendrey, M. J., Faunch, J. A., and Berg, J. M. (1969). Association of D/D translocation with mongolism. Jouranl of Mental Deficiency Research, 13, 89, 98.Google Scholar
Singer, J. D., and Brock, D. J. H. (1971). Half-normal adenylate kinase activily in Three generations. Annals of Human Genetics, 35, 109, 114.CrossRefGoogle Scholar
Smith, G. F. (1967). Correlation of dermal patterns on finger-tips and toes in mongolism. In Mongolism: Ciba Foundation Study Group no. 25, pp. 35–40. Churchill: London.Google Scholar
Smith, G. F., Bat-Miriam, M., and Ridler, M. A. C. (1966). Dermal patterns on the fingers and toes in mongolism. Journal of Mental Deficiency Research, 10, 105–115.Google ScholarPubMed
Smith, G. F., and Berg, J. M. (1968). Dermatoglyphs in Rubinstein-Taybi syndrome. Proceedings of the First Congress of the International Association for the Scientific Study of Mental Deficiency, Montpellier, 1967, pp. 606–619. Edited by Richards, B. W.. Jackson: Reigate.Google Scholar
Smith, G. F., Berg, J. M., Ridler, M. A. C., Faunch, J. A., Farnham, F. N., and Pendrey, M. J. (1967). Familial transmission of an aberrant submetacentric chromosome. Journal of Mental Deficiency Research, 11, 58–68.Google Scholar
Smith, G. F., Kolb, H., and Faunch, J. A. (1968). Spindle bridge and mid-body in cultured lymphocytes. Blood, 31, 175–179.Google Scholar
Smith, G. F., and O'Hara, P. T. (1967). Nuclear pockets in normal leucocytes. Nature, 215, 773.Google Scholar
Smith, G. F., and O'Hara, P. T. (1968). Structure of nuclear pockets in human leukocytes. Journal of Ultrastructure Research, 21, 415–423.Google Scholar
Smith, G. F., Penrose, L. S., and O'Hara, P. T. (1967). Crystalline bodies in lymphocytes of patients with Down's syndrome. Lancet, 2, 452–453.Google Scholar