Výsledky vyhledávání - "F Z, Bischoff"

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study

Autor: D W, Bianchi, J L, Simpson, L G, Jackson, S, Elias, W, Holzgreve, M I, Evans, K A, Dukes, L M, Sullivan, K W, Klinger, F Z, Bischoff, S, Hahn, K L, Johnson, D, Lewis, R J, Wapner, F, de la Cruz

Publikováno v: Prenatal diagnosis. 22(7)

The National Institute of Child Health and Human Development Fetal Cell Isolation Study (NIFTY) is a prospective, multicenter clinical project to develop non-invasive methods of prenatal diagnosis. The initial objective was to assess the utility of f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f661683f84253cc72c95a5d29013bbc3
https://pubmed.ncbi.nlm.nih.gov/12124698

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Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients

Autor: Y, Iitsuka, A, Bock, D D, Nguyen, C A, Samango-Sprouse, J L, Simpson, F Z, Bischoff

Publikováno v: American journal of medical genetics. 98(1)

Klinefelter (47,XXY) syndrome occurs in approximately 1:800 male births and accounts for about 10-20% of males attending infertility clinics. Recent studies have shown no obvious phenotypic differences between subjects in which the extra X-chromosome

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6a92e3994c0b0578fa2419fc9de9830c
https://pubmed.ncbi.nlm.nih.gov/11426451

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Genetic concerns for the subfertile male in the era of ICSI

Autor: E D, Kim, F Z, Bischoff, L I, Lipshultz, D J, Lamb

Publikováno v: Prenatal diagnosis. 18(13)

The treatment of severe male factor infertility has seen remarkable advances in the last five years with the introduction and widespread use of intracytoplasmic sperm injection (ICSI). Although ICSI represents one of the most important advances in th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::58e08e092b47337f01d606c4bff2ce17
https://pubmed.ncbi.nlm.nih.gov/9949435

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Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16

Autor: A S, Schneider, F Z, Bischoff, C, McCaskill, M L, Coady, J E, Stopfer, L G, Shaffer

Publikováno v: American journal of medical genetics. 66(2)

Uniparental disomy for chromosome 16 has been previously identified in fetal deaths and newborn infants with limited follow-up. Thus there is a lack of information about the long-term effects of maternal uniparental disomy 16 on growth and developmen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ea1a163d0cffb9d8f1fc7198827a6a8e
https://pubmed.ncbi.nlm.nih.gov/8958332

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Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry

Autor: D E, Lewis, W, Schober, S, Murrell, D, Nguyen, J, Scott, J, Boinoff, J L, Simpson, F Z, Bischoff, S, Elias

Publikováno v: Cytometry. 23(3)

A noninvasive method of prenatal genetic diagnosis requires fetal cell selection from the maternal circulation that allows efficient recovery for analysis by fluorescence in situ hybridization (FISH). We have solved several problems that negatively a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::08783173f551fcb6b655a859caf1b2e4
https://pubmed.ncbi.nlm.nih.gov/8974867

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