Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D P, Bick"'
Publikováno v:
Journal of Lipid Research, Vol 32, Iss 5, Pp 793-800 (1991)
Rat high density lipoproteins (HDL) were labeled with a series of phosphatidylcholines and ether analogs of phosphatidylcholine. The rates of turnover of the phosphatidylcholine ethers in the rat decreased as a function of increasing hydrophobicity a
Externí odkaz:
https://doaj.org/article/9292e61ad778413c952e87999f5b5d54
Autor:
D. McCorkle, C. M. Meyers, Wayne S. Stanley, Richard I. Kelley, D. P. Bick, H. J. Stern, G. D. Berkovitz, P. Staszak
Publikováno v:
Prenatal Diagnosis. 19:68-71
A cytogenetically normal male fetus was subsequently found to have female external genitalia, a cardiac malformation and mid-trimester intra-uterine growth retardation by ultrasound examination. The maternal serum oestriol level was low. The combinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757a7b2adef870d7f57664e87d039ace
https://doi.org/10.1002/(sici)1097-0223(199901)19:1<68::aid-pd461>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199901)19:1<68::aid-pd461>3.0.co
Autor:
J C, Achermann, W X, Gu, T J, Kotlar, J J, Meeks, L P, Sabacan, S B, Seminara, R L, Habiby, P C, Hindmarsh, D P, Bick, R J, Sherins, W F, Crowley, L C, Layman, J L, Jameson
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(12)
Although delayed puberty is relatively common and often familial, its molecular and pathophysiologic basis is poorly understood. In contrast, the molecular mechanisms underlying some forms of hypogonadotropic hypogonadism (HH) are clearer, following
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::943c4f73919f1a67b52fb9424d52ba10
https://pubmed.ncbi.nlm.nih.gov/10599708
https://pubmed.ncbi.nlm.nih.gov/10599708
Autor:
W C, Spence, S H, Black, L, Fallon, A, Maddalena, E, Cummings, G, Menapace-Drew, D P, Bick, G, Levinson, J D, Schulman, P N, Howard-Peebles
Publikováno v:
American journal of medical genetics. 64(1)
In December, 1993, we initiated a pilot project in which DNA fragile X (fraX) testing was offered during routine prenatal or genetic counseling to all pregnant women seen at the GeneticsIVF Institute, most of whom were referred for the indication of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::308698220cb4e78e0e333b3e70137d43
https://pubmed.ncbi.nlm.nih.gov/8826471
https://pubmed.ncbi.nlm.nih.gov/8826471
Publikováno v:
Transfusion. 34(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36deaaf6d201b38d4f045f9031165644
https://pubmed.ncbi.nlm.nih.gov/8073496
https://pubmed.ncbi.nlm.nih.gov/8073496
Publikováno v:
The Journal of reproductive medicine. 37(5)
DNA-based testing is becoming possible for an increasing number of hereditary diseases as the responsible genes are mapped to individual chromosomes and then isolated and characterized. The strategy for each test depends on the heterogeneity of mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7897603d820458ebc9ed0fe76ec2fdef
https://pubmed.ncbi.nlm.nih.gov/1507192
https://pubmed.ncbi.nlm.nih.gov/1507192
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Publikováno v:
Prenatal Diagnosis. 7:543-549
We describe a fetus with epidermolysis bullosa dystrophica and a fetus with aplasia cutis congenita who were normal by careful ultrasound examination but whose midtrimester amniotic fluids exhibited elevated concentrations of alpha-fetoprotein and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2394a2a0d0ad421852a75848cab34b94
https://doi.org/10.1002/pd.1970070803
https://doi.org/10.1002/pd.1970070803