Zobrazeno 1 - 10
of 14
pro vyhledávání: '"M S, Verp"'
Publikováno v:
The Journal of reproductive medicine. 42(2)
To determine the effect of reports and media coverage on chorionic villus sampling (CVS) and limb reduction defects (LRD) on patients' utilization of CVS for prenatal testing for advanced maternal age and to quantitate the relation of preferences for
Autor:
S L, Christian, A C, Smith, M, Macha, S H, Black, F F, Elder, J M, Johnson, R G, Resta, U, Surti, L, Suslak, M S, Verp, D H, Ledbetter
Publikováno v:
Prenatal diagnosis. 16(4)
Maternal uniparental disomy 15 (UPD15), responsible for approximately 25 per cent of Prader-Willi syndrome cases, is usually caused by maternal meiosis I non-disjunction associated with advanced maternal age. These cases may initially be detected as
Publikováno v:
Journal of lipid research. 36(8)
Apolipoprotein (apo) B mRNA editing is a site-specific cytidine deamination reaction responsible for the production of apoB-48 in mammalian small intestine. This process is mediated by an enzyme complex that includes the catalytic subunit, APOBEC-1.
Publikováno v:
American journal of obstetrics and gynecology. 168(3 Pt 1)
Our purpose was to assess the presence and frequency of gamma delta T cells in the decidua of term and first-trimester pregnancies.Term and first-trimester placentas were obtained from normal subjects. Frozen sections and cell suspensions were prepar
Publikováno v:
Cancer. 66(12)
The first case (to the authors' knowledge) is reported of a true hermaphrodite with bilateral ovotestes, bilateral gonadoblastomas and dysgerminomas, a 46, XX/46,XY karyotype, and a successful pregnancy. The true hermaphroditism was diagnosed during
Autor:
M S, Verp, N L, Unger
Publikováno v:
Journal of perinatology : official journal of the California Perinatal Association. 10(1)
Chorion, placental membranes, and embryo all arise from the same fertilized oocyte; therefore, chorionic cells are presumed to reflect fetal chromosome status. Progenitor cells of the embryo are selected from the blastocyst, however, at a very early
Publikováno v:
Genetics in Medicine. 1:64
We report one fetus of a twin pregnancy with a de novo unbalanced translocation detected by elevated maternal serum alpha-fetoprotein(MSAFP) and an abnormal ultrasound examination. A 33 year old African female was referred for genetic counseling at 1
Publikováno v:
Journal of Perinatal Medicine; Nov2003, Vol. 31 Issue 6, p535-537, 3p
Publikováno v:
Obstetrics and gynecology. 62(4)
After observing abnormal offspring following artificial insemination by donor, several authors recently have proposed intensive genetic screening of donors. The screening would be beyond that practiced by most infertility specialists. To determine th
Autor:
M S, Verp, A P, Amarose
Publikováno v:
The Journal of reproductive medicine. 32(6)
An abnormal sex chromosome constitution (45,X/46,XX) was observed in a woman with Crohn's disease and multiple spontaneous abortions. Immunologic disorders, inflammatory bowel disease and X chromosome abnormalities appear to be positively associated.