Zobrazeno 1 - 10 of 25 pro vyhledávání: '"M. A. C. Ridler"'
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A balanced autosomal translocation (3;9) associated with primary hypogonadism and dorsal spine stenosis
Autor: M. A. C. Ridler, P. J. Hughes, J. M. R. Edwards, R. J. M. Lane
Publikováno v: Clinical genetics. 43(1)
A man with a balanced translocation between chromosomes 3 and 9 associated with primary hypogonadism and dorsal spine stenosis is reported. The possible significance of this chromosomal abnormality is discussed.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ded036deffa69b3ade6643eead67b276
https://pubmed.ncbi.nlm.nih.gov/8462195
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5
Segregation of ABO, AK1and ACONSin families with abnormalities of chromosome 9
Autor: K. E. Buckton, J. Insley, M. A. C. Ridler, E. B. Robson, Maj Hultén, P. J. L. Cook, C. E. Blank, C. A. Slaughter, J. E. Gray, F. E. James
Publikováno v: Annals of Human Genetics. 41:365-377
SUMMARY Some families with abnormalities of chromosome 9 have been combined with others from the literature to show that AK1 and ABO must lie near the end of that chromosome. Current evidence suggests that both lie in band 9q34. MNSs, GPT and Gc can
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab32bab9bb68491a5741c4a8a4bfcfe4
https://doi.org/10.1111/j.1469-1809.1978.tb01904.x
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6
An etiological survey of the severely retarded Hertfordshire children who were born between January 1, 1965 and December 31, 1967
Autor: Renata Laxova, M. A. C. Ridler, Marry Bowen-Bravery, J. M. Opitz
Publikováno v: American Journal of Medical Genetics. 1:75-86
An etiological survey is presented of all suveryl retarded children living in Hertfordshire, at home and in residential care, born between January 1, 1965, and December 31, 1967. One hundred and forty-six children (87 boys and 59 girls) were ascertai
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::112e6e04764f91f9cc6f86c086c99dc4
https://doi.org/10.1002/ajmg.1320010109
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8
Family with probable achondrogenesis and lipid inclusions in fibroblasts
Autor: Renata Laxova, M. A. C. Ridler, J. A. D. Timothy, Peter T. Ohara
Publikováno v: Archives of Disease in Childhood. 48:212-216
Three stillborn sibs, two males and a female, with probable achondrogenesis, whose parents are first cousins, are reported. Fibroblast cultures revealed numerous large intracellular lipid inclusions in the two stillborns, which were available for inv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c25cca314f3822b682a8f0cf92f5869
https://doi.org/10.1136/adc.48.3.212
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10
Sex Chromatin Abnormalities in Female Subnormal Patients
Autor: W. R. McKIBBEN, A. Shapiro, M. A. C. Ridler
Publikováno v: British Journal of Psychiatry. 109:390-394
This survey is the concluding part of an investigation of the distribution of abnormalities of the sex chromatin body in the whole of the patient population of Harperbury Hospital. The results of the survey of the male patients of the hospital have a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::627a82e7398b9fa3bb9b11f0ba142da1
https://doi.org/10.1192/bjp.109.460.390
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