Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jerome L. McCombs"'
Publikováno v:
British Journal of Haematology. 85:627-630
Summary. Patients with Fanconi's anaemia (FA) have aplastic anaemia, leukaemia, myelodysplasia and tumours. Since leukaemia has a very poor prognosis, it is desirable to identify high-risk patients. To determine the significance of clonal marrow chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2c1da456b9d0a6a98ef20fcbb9eed4
https://doi.org/10.1111/j.1365-2141.1993.tb03362.x
https://doi.org/10.1111/j.1365-2141.1993.tb03362.x
Autor:
Ching Chyuan Hsieh, John Papaconstantinou, Jerome L. McCombs, Michael J. Keherly, Linda S. Merryman
Publikováno v:
Somatic Cell and Molecular Genetics. 22:119-134
We utilized an AFP-HPRT transgene, i.e. the HPRT coding sequences under the regulation of AFP enhancer and promoter sequences, to localize the AFP extinguisher locus in intertypic somatic cell hybrids (hepatoma X fibroblast). This hybrid gene constru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f26ce21a284fbf2e7ef60745f71fcbd
https://doi.org/10.1007/bf02369902
https://doi.org/10.1007/bf02369902
Autor:
Marguerite A. Sognier, George Lynch, Richard L. Eberle, Monique Tucker, Jerome L. McCombs, James A. Belli, David Brown
Publikováno v:
Genetic Analysis: Biomolecular Engineering. 11:69-76
The potential usefulness of chromosome microdissertion, the polymerase chain reaction (PCR), and dot blot hybridization as a quick screening method for determining the genetic composition of double minute chromosomes (DMs) was evaluated. DMs or abrno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b88d1a8fda03a16d2920541b8ae95c0
https://doi.org/10.1016/1050-3862(94)90053-1
https://doi.org/10.1016/1050-3862(94)90053-1
Publikováno v:
The American Journal of Cardiology. 79:388-390
Two patients with cervical aortic arch are described, both with deletions in chromosome 22q11 region, and thymic hypofunction. This suggests that cervical aortic arch is part of the spectrum of the CATCH 22 group of defects.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4afdd10b12ed987b357bcc3cd4f19ab0
https://doi.org/10.1016/s0002-9149(96)00772-2
https://doi.org/10.1016/s0002-9149(96)00772-2
Autor:
L.H.S. Van Mierop, H. K. Hawkins, David W. Sapire, Anil Kumar, Jerome L. McCombs, Lillian H. Lockhart
Publikováno v:
American Journal of Medical Genetics. 61:89-91
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2e1326d884e1b8ceb389625f6893927
https://doi.org/10.1002/ajmg.1320610104
https://doi.org/10.1002/ajmg.1320610104
Autor:
Jerome L. McCombs, Glennda M. Rassin
Publikováno v:
Clinical Pediatrics. 32:382-384
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fa3bb0713f6aa08244d0fc564c70207
https://doi.org/10.1177/000992289303200618
https://doi.org/10.1177/000992289303200618
Publikováno v:
Experimental cell research. 205(2)
We describe a sequential staining technique for the karyotypic analysis of interspecific mouse × human somatic cell hybrids. Fluorescence in situ hybridization of samples, previously stained using standard trypsin/Giemsa protocols, was instrumental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da1464d9c6476b5b20a9f6ffc836762
https://pubmed.ncbi.nlm.nih.gov/8482340
https://pubmed.ncbi.nlm.nih.gov/8482340
Publikováno v:
Cancer genetics and cytogenetics. 50(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22c8f357b32db0c7caaa534cf3c12bf0
https://pubmed.ncbi.nlm.nih.gov/2253186
https://pubmed.ncbi.nlm.nih.gov/2253186
Autor:
Jerome L. McCombs, Anil Kumar, Edward G. Brooks, Frank C. Schmalstieg, Ruksana Huda, David W. Sapire, Bruce S. Keenan
Publikováno v:
Pediatric Research. 41:23-23
Recent observations of deletion in chromosome 22q11 in patients with conotruncal heart defects (CHD) has led to suggestions that these patients belong to the CATCH 22 group of defects. Subtle abnormalities of T-cell numbers and low levels of parathor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4ea8fe182958097008b555908d6e422
https://doi.org/10.1203/00006450-199704001-00142
https://doi.org/10.1203/00006450-199704001-00142
Publikováno v:
Pediatric Research. 39:31-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91bd2736424513f03509800b51acc647
https://doi.org/10.1203/00006450-199604001-00188
https://doi.org/10.1203/00006450-199604001-00188