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Akademický článek
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Publikováno v:
Journal of Cell Science. 36:215-221
Patterns of chromosome segregation were studied in 2 different intraspecific mouse cell hybrids: (1) A9 × B82, formed by fusing 2 cell lines of heteroploid fibroblasts, and (2) UWE, originating from the fusion of A9 cells with euploid foetal erythro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4ccb6152107ecd39039b1e45fbe7c24
https://doi.org/10.1242/jcs.36.1.215
https://doi.org/10.1242/jcs.36.1.215
Publikováno v:
Pediatrics. 56:826-831
In 1970 we reported the case of a 2-month-old boy with a C autosomal trisomy and euploid mosaicism, and suggested, by comparison with other cases, that this chromosome imbalance might result in a definite syndrome. It has now been determined by Giems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfcfb987a1e6a5331d4fa50fa1ae6ac9
https://doi.org/10.1542/peds.56.5.826
https://doi.org/10.1542/peds.56.5.826
Publikováno v:
Journal of Cell Science. 25:59-71
Hybrids between A9 (HGPRT-) and B82 (TK-), mouse heteroploid fibroblast lines, were obtained through continuous cultivation and clonal selection; such hybrids showed marked segregation and by conventional stains displayed chromosome numbers and distr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e478ab1f4666a4c1286bb28686f27995
https://doi.org/10.1242/jcs.25.1.59
https://doi.org/10.1242/jcs.25.1.59
Publikováno v:
New England Journal of Medicine. 273:738-742
ALTERATIONS of smaller acrocentric chromosomes in malignant blood diseases have drawn much attention ever since the Philadelphia (PH1) chromosome was noted in chronic myelogenous leukemia.1 , 2 In 1962 Atkin and Taylor3 described a fifty-three-year-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::108df62fcf3b3046ed5bc4f72170c67f
https://doi.org/10.1056/nejm196509302731404
https://doi.org/10.1056/nejm196509302731404
Publikováno v:
The New England journal of medicine. 291(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe2e963b7cd8c48feb189819222481c2
https://pubmed.ncbi.nlm.nih.gov/4525414
https://pubmed.ncbi.nlm.nih.gov/4525414
Publikováno v:
The New England journal of medicine. 296(22)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b990731f4a514cd7692be4812ff78c47
https://pubmed.ncbi.nlm.nih.gov/266114
https://pubmed.ncbi.nlm.nih.gov/266114
Publikováno v:
The American journal of medicine. 40(2)
A sixteen year old girl is described who had typical features of pycnodysostosis, a genetically determined disorder of bone which usually is inherited as a Mendelian recessive trait. The clinical findings included short stature, separated cranial sut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac2dc07ac777ad3318a2b1c0d42e6955
https://pubmed.ncbi.nlm.nih.gov/5902268
https://pubmed.ncbi.nlm.nih.gov/5902268
Publikováno v:
Southern medical journal. 64(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64c845fe57538a52e065b75aa540610
https://pubmed.ncbi.nlm.nih.gov/5541078
https://pubmed.ncbi.nlm.nih.gov/5541078