Zobrazeno 1 - 10
of 10
pro vyhledávání: '"C. J. English"'
Autor:
C. J. Napier, H. M. Cameron, C J English, G. Linton, N. W. S. Atkey, G. C. Mason, B. J. Murray
Publikováno v:
Prenatal Diagnosis. 20:917-920
A case is reported of a 35-year-old woman who underwent a chorion villus biopsy (CVB) at 17 weeks' gestation after intrauterine growth retardation and oligohydramnios were diagnosed by ultrasound scan. Chromosome analysis of the CVB direct preparatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57a3157f0b1a3baeb4ff38cdfeb7a407
https://doi.org/10.1002/1097-0223(200011)20:11<917::aid-pd937>3.0.co
https://doi.org/10.1002/1097-0223(200011)20:11<917::aid-pd937>3.0.co
Autor:
C. Court-Brown, W. A. Wallace, C. J. English, R. J. Graves, C. A. Soutar, S. P. F. Hughes, R. W. Porter, W. M. Maclaren, A. J. Pethick
Publikováno v:
American Journal of Industrial Medicine. 27:75-90
To make a preliminary assessment of whether upper limb soft tissue disorders might be associated with activities at work, we have conducted a case-control study of subjects attending orthopedic clinics in three cities. All subjects between the ages o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a1c161ded4a0894b068aac02d159e16
https://doi.org/10.1002/ajim.4700270108
https://doi.org/10.1002/ajim.4700270108
Publikováno v:
Prenatal Diagnosis. 12:1067-1071
Direct preparations and long-term cultures from a chorion villus biopsy, taken because of a known maternal additional marker chromosome, showed a 48,XX,+mar,+mar karyotype in all cells examined. The same karyotype was revealed in a subsequent amnioti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1571f026d973862ffb298da8de37c81
https://doi.org/10.1002/pd.1970121214
https://doi.org/10.1002/pd.1970121214
Publikováno v:
Prenatal diagnosis. 20(11)
A case is reported of a 35-year-old woman who underwent a chorion villus biopsy (CVB) at 17 weeks' gestation after intrauterine growth retardation and oligohydramnios were diagnosed by ultrasound scan. Chromosome analysis of the CVB direct preparatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cdca62f337ad44ec441f4f40b393c2c7
https://pubmed.ncbi.nlm.nih.gov/11113896
https://pubmed.ncbi.nlm.nih.gov/11113896
Publikováno v:
Prenatal Diagnosis. 28:266-267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::500aa216ed466bdb7842d840623ab15a
https://doi.org/10.1002/pd.1961
https://doi.org/10.1002/pd.1961
A case of blepharophimosis, ptosis, and epicanthus inversus (BPES) associated with prenatally diagnosed diaphragmatic hernia and interstitial deletion of the long arm of chromosome 3, del(3)(q21q23), is reported. Comparison with other cases of BPES r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d200d7a2cfb18b1a7b3b7f4228e279d1
https://europepmc.org/articles/PMC1050030/
https://europepmc.org/articles/PMC1050030/
Autor:
C J English
Publikováno v:
Nursing Standard. 13:28-28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d180d1c0f28ba7d383f631118d7378b9
https://doi.org/10.7748/ns.13.47.28.s44
https://doi.org/10.7748/ns.13.47.28.s44
Publikováno v:
Journal of medical genetics. 26(6)
Karyotypes were examined in 512 (91.9%) of 557 male patients in an institution for the mentally handicapped. A total of 110 (21.5%) had an abnormal karyotype: 65 (12.7%) with Down's syndrome, 30 (5.9%) with the fragile X syndrome, 13 (2.5%) with auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7782f38046a6eb656a38f87d007bc5ba
https://pubmed.ncbi.nlm.nih.gov/2525623
https://pubmed.ncbi.nlm.nih.gov/2525623
Autor:
T, Jagannathan, J, Foote, V C, Abrahams, A W, Bruce, R F, Hetherington, D W, Lywood, C J, English
Publikováno v:
Investigative urology. 7(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a4338ec15460a768f15d76f0932c2079
https://pubmed.ncbi.nlm.nih.gov/5794215
https://pubmed.ncbi.nlm.nih.gov/5794215
Publikováno v:
Scopus-Elsevier
We present the case of a mentally normal 7 year old girl with short stature, scoliosis, atrial septal defect, and dysmorphic features including linear pigmented streaks on the forearms and lower legs. Chromosome analysis of cultured fibroblasts showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7883faeb47598fa51baff97213034eae
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028211039&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028211039&partnerID=MN8TOARS