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Obstetrics and Gynecology|June 1, 1990
Dilation and evacuation for second-trimester genetic pregnancy terminationL P Shulman, F W Ling, C M Meyers, et al.
American Journal of Medical Genetics|June 28, 2001
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patientsY Iitsuka, A Bock, D D Nguyen, et al.
American Journal of Obstetrics and Gynecology|May 1, 1990
Fetomaternal transfusion depends on amount of chorionic villi aspirated but not on method of chorionic villus samplingL P Shulman, C M Meyers, J L Simpson, et al.
Science (New York, N.Y.)|October 6, 1978
Genetically determined sex-reversal in 46,XY humansJ German, J L Simpson, R S Chaganti, et al.
Advances in Contraception : the Official Journal of the Society for the Advancement of Contraception|December 24, 1997
The frequency and spectrum of congenital anomalies in natural family planning users in South America: no increase in a case-control study. NFP-ECLAMC Group. Natural Family Planning. Latin-American Collaborative Study of Congenital MalformationsE E Castilla, J S Lopez-Camelo, M da Graça Dutra, et al.
American Journal of Obstetrics and Gynecology|December 1, 1995
Associations between adverse perinatal outcome and serially obtained second- and third-trimester maternal serum alpha-fetoprotein measurementsJ L Simpson, G E Palomaki, B Mercer, et al.
Clinical Genetics|August 1, 1977
An autosomal dominant midline cleft syndrome resembling familial holoprosencephalyA O Martin, J C Perrin, W A Muir, et al.
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