Zobrazeno 1 - 10
of 12
pro vyhledávání: '"N L, Rudd"'
Publikováno v:
Prenatal diagnosis. 10(5)
Amniocentesis was performed because of a fetal abdominal wall defect, and a 45,X karyotype was obtained. A near-normal male infant with no features of Turner syndrome was delivered. The karyotype of the infant was 45,X/46,X, dic(Y)(q11), with each of
Publikováno v:
Journal of Medical Genetics. 14:430-437
This paper describes 6 individuals, occurring in 3 generations of a single family, who were affected by a distinct syndrome which included: retardation and microcephaly; a small oval face with almond-shaped eyes, droopy eyelids, a small nose, and sma
Autor:
N L, Rudd, B M, Youson
Publikováno v:
L' Infirmiere canadienne. 19(1)
Publikováno v:
Genome. 32(2)
Spontaneous micronucleus frequencies were measured in 11 human fibroblast strains, with early-passage cells that had never been frozen and with cells of comparable population doublings that had been cryopreserved in liquid nitrogen. The mean micronuc
Publikováno v:
Birth defects original article series. 13(3D)
Publikováno v:
Birth defects original article series. 14(6C)
Autor:
N J, Howard, N L, Rudd
Publikováno v:
Birth defects original article series. 13(3C)
A boy whose mother ingested aminopterin to induce abortion and who has the characteristic anomalies caused by fetal exposure to this drug, has been followed for 12.75 yr. Despite short stature, his growth velocity is normal, and both normal endocrine
Autor:
N L, Rudd, B M, Youson
Publikováno v:
The Canadian nurse. 72(8)
The problems faced by a couple undergoing amniocentesis to test for genetic disorders, the guilt feelings associated with a dicision to abort a defective fetus, and the role of the nurse at the genetic clinic in helping at this difficult time are exa
Publikováno v:
Obstetrics and gynecology. 60(2)
Amniotic fluid alpha-fetoprotein (AFP) assays and detailed ultrasound examinations were performed in 376 prenatal patients at risk for a neural tube defect (high-risk group). In addition, 2436 patients who underwent amniocentesis for other indication
Autor:
R, Benzie, T A, Doran, W, Escoffery, H A, Gardner, D I, Hoar, A, Hunter, R, Malone, M, Miskin, N L, Rudd
Publikováno v:
Birth defects original article series. 12(6)