Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Autor: Bogart, M H, Bradshaw, C L, Jones, O W, Schanberger, J E

Publikováno v: Journal of Medical Genetics; Apr1986, Vol. 23 Issue 2, p180-183, 4p

REPORT OF THE ACM NOMINATING COMMITTEE.

Autor: Bradshaw, C. L., Armer, Paul, Forsythe, George

Publikováno v: Communications of the ACM. Mar1968, Vol. 11 Issue 3, p204-204. 1/3p.

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Autor: Hsu LY; Prenatal Diagnosis Laboratory of New York City/Medical and Health Research Association of N.Y., Inc., NY, USA., Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P

Publikováno v: Prenatal diagnosis [Prenat Diagn] 1997 Mar; Vol. 17 (3), pp. 201-42.