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A General Introduction
The Possible Use of Amniocentesis for Monitoring
II Classification and Tabulation
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abortuses agents allele analysis anencephaly approach automated biochemical birth defects breakage cancer cells ceruloplasmin changes chemical chromatid clinical collection congenital anomalies congenital malformations crease crown-rump crown-rump length cytogenetic dermatoglyphic detection diagnosis disease disorders effects electrophoretic embryos and fetuses environmental enzyme estimated evaluation examined factors fetal frequency gene germinal mutation gestational Health hemoglobin hospital Hum Genet Human Population identify incidence increase individual infants investigators karyotype laboratory large number linkage major malformations marker material methods minor anomalies minor birth defects mutagenesis mutagens mutation rate National newborn nondisjunction nonpaternity normal observed parents patient patterns phenotype physician possible pregnancy problem proteins quantitative rare variants registry reported rubella samples screening serum sex ratio somatic mutations specific specimens spina bifida spontaneous abortions studies surveillance syndrome techniques teratogenesis teratogens Teratology thalidomide therapeutic tion transferrin variables vital records Weitkamp York