Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Felice M. Weber"'
Publikováno v:
Clinical Genetics. 3:264-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e2495dcf8e5e51fb2153a760676811
https://doi.org/10.1111/j.1399-0004.1972.tb04275.x
https://doi.org/10.1111/j.1399-0004.1972.tb04275.x
Publikováno v:
Blood. 41:259-263
The occurrence of acute lymphocytic leukemia in a young man with a C-G translocation is described. Two members of his family also show C-G translocations but have not as yet developed leukemia. A third member of the family, on whom no chromosomal inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc8a0a5d05342fbe5fe4657b23187eea
https://doi.org/10.1182/blood.v41.2.259.259
https://doi.org/10.1182/blood.v41.2.259.259
Autor:
Helga Muller, John J. Hutton, Angela Rocchi, J.H. Smith, Rhea Stewart, M.S. Grewal, Adriana de Capoa, Frederick Hecht, T.H. Yosida, Dorothy A. Miller, H.E. Wyandt, E.W. Lovrien, V.G. Dev, O.J. Miller, H. Kato, R. S. Sparkes, Felice M. Weber, R.E. Kouri, T.J. Marlowe
Publikováno v:
Cytogenetic and Genome Research. 10:I-VII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::167b3617a960aca1a4151dae08a650b4
https://doi.org/10.1159/000130158
https://doi.org/10.1159/000130158
Publikováno v:
The Journal of Pediatrics. 76:594-597
A 2 1/2-year-old girl had anal atresia, bilateral microphthalmia, and preauricular skin tags. Her clinical pattern resembled that of 6 reported cases, all of which had an extra small acrocentric chromosome. Chromosome analysis revealed a similar extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291f67f45d15132ad6576907715f7746
https://doi.org/10.1016/s0022-3476(70)80410-3
https://doi.org/10.1016/s0022-3476(70)80410-3
Publikováno v:
American Journal of Obstetrics and Gynecology. 107:1092-1098
The clinical and cytogenetic heterogeneity of gonadal dysgenesis is illustrated by three patients who have a partially deleted X chromosome in some or all of their cells. Their variable findings emphasize the need for extensive evaluations in patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4cd0a784edb51d7d8541d97c8536fe
https://doi.org/10.1016/0002-9378(70)90634-4
https://doi.org/10.1016/0002-9378(70)90634-4
Publikováno v:
Journal of Medical Genetics. 10:177-179
A four-year-old girl with typical Down's syndrome is described. She has 47,XX,+21 karyotype in skin and lymphocytes and 47,XX,+mar karyotype in some lymphocytes. Autoradiography and fluorescent analyses have failed to identify the +mar chromosome whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2139cbb328499608b8d1f2b880be8b0b
https://doi.org/10.1136/jmg.10.2.177
https://doi.org/10.1136/jmg.10.2.177
Publikováno v:
Cytogenetics. 10(6)
Double monosomy mosaicism was observed in a three-year-old girl who had mental and physical retardation. Routine blood-lymphocyte and bone-marrow chromosome studies showed an apparent 45, X pattern, which was confirmed by autoradiographic studies wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58bcd288eab754f160e281d30d0d7835
https://pubmed.ncbi.nlm.nih.gov/5146417
https://pubmed.ncbi.nlm.nih.gov/5146417
Autor:
M.S. Grewal, T.H. Yosida, Felice M. Weber, H. Kato, V.G. Dev, H.E. Wyandt, O.J. Miller, John J. Hutton, Helga Muller, Angela Rocchi, R.E. Kouri, Dorothy A. Miller, Adriana de Capoa, Rhea Stewart, Frederick Hecht, E.W. Lovrien, T.J. Marlowe, R. S. Sparkes, J.H. Smith
Publikováno v:
Cytogenetic and Genome Research. 10:472-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc9f70f48000e0b3a1e2c8bb2624cbff
https://doi.org/10.1159/000130169
https://doi.org/10.1159/000130169