What people are saying - Write a review
We haven't found any reviews in the usual places.
CONGENITAL MALFORMATIONS SOME GENETIC
RECENT DEVELOPMENTS IN SOMATIC CELL GENETICS
6 other sections not shown
aciduria active affected alleles amino acids aminoacidopathies amniocentesis amniotic fluid anencephaly anomalies autosomal banding blastocyst blood and urine branched-chain child chromo chromosomal abnormalities chromosome number clinical culture Cytogenetics deficiency dehydrogenase deleted diagnosis differentiation Down's Syndrome early ectodermal ridge elevated blood embryos environmental enzyme factors families Feeding difficulty female fertilization fetal fetus fibroblasts fluorescent function G6PD genetic counseling genetic disease genitalia genotype gestation heterozygous human chromosome human genetic disease hybrid hyperammonemia inactivation individuals inherited metabolic involves laboratory limb loci locus major male mammalian maternal mechanisms meiotic metabolic diseases molecules mouse multifactorial mutant gene neonatal neural plate neural tube defects newborn normal occur offspring oocytes oogenesis organisms parents patients phenotype polygenic polyploidization population pregnancy prenatal present protein quinacrine recently recessive recurrence risks restriction of protein result sex chromosomes single gene specific structure studies tion tissues translocation trisomy virilization virus X-chromosome X-linked Yes Dietary restriction