Zobrazeno 1 - 8
of 8
pro vyhledávání: '"W E, Crowder"'
Autor:
Velma Paschall, B. Lubianski, David H. Ledbetter, W. E. Crowder, Frank Greenberg, J. Colon-Linares
Publikováno v:
Human Genetics. 65:317-319
Partial monosomy of 22q due to an unbalanced 4;22 translocation was seen in a 2-month-old male with Type I truncus arteriosus, dysmorphic features, and T-cell abnormalities. The family history revealed a previous sib with Type I truncus arteriosus, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e726ebe474cec7cbbfaf530d91a648be
https://doi.org/10.1007/bf00291554
https://doi.org/10.1007/bf00291554
Publikováno v:
Birth defects original article series. 18(3 Pt)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f18a5efa047e8cd80fa493c5cdeaf04d
https://pubmed.ncbi.nlm.nih.gov/7126787
https://pubmed.ncbi.nlm.nih.gov/7126787
Autor:
W E, Crowder, F L, Shannon
Publikováno v:
Obstetrics and gynecology. 61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b06dfb3d5fab29d264f1c636092317e3
https://pubmed.ncbi.nlm.nih.gov/6823394
https://pubmed.ncbi.nlm.nih.gov/6823394
Autor:
W E, Crowder, I M, Schulman
Publikováno v:
CDA journal. 10(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31aba5c27084844eea7a9f207e319135
https://pubmed.ncbi.nlm.nih.gov/6959705
https://pubmed.ncbi.nlm.nih.gov/6959705
Publikováno v:
Ophthalmology. 91(8)
Gardner syndrome is a dominantly inherited familial cancer syndrome characterized by intestinal polyposis, bony hamartomata, and various soft tissue tumors. The risk of malignancy during adult life is essentially 100%, but as yet no phenotypic marker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db9745375ac3878a42c77afb5e52073e
https://pubmed.ncbi.nlm.nih.gov/6493700
https://pubmed.ncbi.nlm.nih.gov/6493700
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 80(13)
Using cloned cDNA sequences of murine and human hypoxanthine phosphoribosyltransferase (HPRT: IMP: pyrophosphate phosphoribosyltransferase, EC 2.4.2.8), we have identified and characterized a three-allele restriction-fragment-length polymorphism for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab15f3c3afad58aa2b7407fd93583e88
https://pubmed.ncbi.nlm.nih.gov/6306659
https://pubmed.ncbi.nlm.nih.gov/6306659
Autor:
W. E. Crowder, E. N. Smith
Publikováno v:
Journal of Applied Physiology. 36:634-635
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8630f9bacc920340316f862d9b255274
https://doi.org/10.1152/jappl.1974.36.5.634
https://doi.org/10.1152/jappl.1974.36.5.634
Autor:
W. E. Crowder
Publikováno v:
The Downside Review. 73:311-312
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50a9f391c065f336be9b084865a72eaa
https://doi.org/10.1177/001258065507323325
https://doi.org/10.1177/001258065507323325