Zobrazeno 1 - 10
of 88
pro vyhledávání: '"E. Lenzini"'
Publikováno v:
Annales de genetique. 34(1)
The authors report on cytogenetic results of six patients with hypomelanosis of Ito. Karyotypes from peripheral lymphocytes prometaphases and skin fibroblasts metaphases were normal. A review of the literature revealed no specific chromosomal abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6bbe4d34a55da4d758152995aa10e8c3
https://pubmed.ncbi.nlm.nih.gov/1952789
https://pubmed.ncbi.nlm.nih.gov/1952789
Autor:
E. Piovan, D. Heller, P. Kahn, S. Shin, G. Goppion, S.S. Tevethia, Colin V. Beechey, F. Anglani, R.A. Mulivor, Maggie Kirk, Frank H. Ruddle, P.W. Melera, Warren W. Nichols, U.H. Wiberg, Joseph P. Davide, L.L. Coriell, L. Artifoni, A.E. Greene, V.J. Goyanes, C. Baccichetti, M. Roberts, Edward P. Evans, M.M. Aronson, E. Lenzini, J.B. Schvartzman, K.-H. Choi, Dirk G. de Rooij, M.L. Figueroa, A.G. Searle, R. Tenconi, J.T. Hart, B.K. Vig, L. Christidis, P. de Boer
Publikováno v:
Cytogenetic and Genome Research. 36:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f0f946f5b892c844904996e074529e4
https://doi.org/10.1159/000131980
https://doi.org/10.1159/000131980
Publikováno v:
Annales de genetique. 31(3)
Three subjects from 2 unrelated families with partial duplication of 17q, derived from a reciprocal parental translocation between chromosomes 11 and 17 with different breakpoints, are described. A female patient from one family with a 46,XX,-11,+der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e98812db9daf73d825ffee7f5363ed53
https://pubmed.ncbi.nlm.nih.gov/3265610
https://pubmed.ncbi.nlm.nih.gov/3265610
Publikováno v:
Pathologica. 71(1013)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6d4704a40f62ae947438d7c47a46d64
https://pubmed.ncbi.nlm.nih.gov/548895
https://pubmed.ncbi.nlm.nih.gov/548895
Autor:
C, Baccichetti, E, Lenzini, P, Temperani, R, Pallotta, P L, Giorgi, E, Tarantino, G, Mengarda, B, Dordi
Publikováno v:
Annales de genetique. 22(4)
A study of three new cases with different trisomies involving chromosome 9 and a review of about 100 cases of partial trisomy 9 reported in the literature, suggested some cytogenetical and clinical correlations and lead us to propose the nomenclature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd0a680a2765f8d62a9512ce96e98c58
https://pubmed.ncbi.nlm.nih.gov/399166
https://pubmed.ncbi.nlm.nih.gov/399166
The DNA replication patterns of eight cases of X isochromosomes, five idic(X) and three i(Xq), were studied. R-banded prometaphases and metaphases from lymphocyte cultures after synchronization with methotrexate and incorporation of 5-bromodeoxyuridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d4fc5b602db19e784620186384e6054
http://hdl.handle.net/11577/2505525
http://hdl.handle.net/11577/2505525
Autor:
A, Drusini, E, Lenzini
Publikováno v:
Acta anthropogenetica. 7(3)
Dermatoglyphic data on six cases of 9p syndrome (trisomy of the short arm of chromosome 9), compared with those from the published literature, are presented. Some dermatoglyphic features appear to recur in all cases, suggesting their use in diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbc2f41ca583c8c1031188a60f0e83c6
https://pubmed.ncbi.nlm.nih.gov/6680661
https://pubmed.ncbi.nlm.nih.gov/6680661
Publikováno v:
Pathologica. 71(1013)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af8e6f06a6b722e981b7b8e4aa86344a
https://pubmed.ncbi.nlm.nih.gov/548872
https://pubmed.ncbi.nlm.nih.gov/548872
Autor:
C, Baccichetti, E, Lenzini
Publikováno v:
Minerva urologica e nefrologica = The Italian journal of urology and nephrology. 37(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c814634972f073960dc43cbdc96326cf
https://pubmed.ncbi.nlm.nih.gov/3834620
https://pubmed.ncbi.nlm.nih.gov/3834620