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Introduction to Genetics
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affected child affected persons amniocentesis amniotic fluid anencephaly anomalies approximately associated autosomal dominant autosomal dominant inheritance autosomal dominant mode autosomal recessive autosomal recessive mode baby birth defects cancer Carrier detection cataracts Chapter characterized chromosome abnormalities cleft Clin clinical manifestations condition couple cytogenetic deafness deficiency deletion diabetes disorders Down's syndrome drome drugs dysplasia Engl enzyme evaluation females fetal fetoscopy follows an autosomal frequently genetic counseling genetic disease Gynecol hemoglobin Hereditary increased risk individuals infection involves isolated defect karyotype leukemia males malformations malignant maternal Mendelian mental retardation metabolic microcephaly mode of inheritance mosome muscle muscular dystrophy mutation normal Obstet occur onset palate parents Pediatr phenotype Potentially possible pregnancy Prenatal diagnosis recurrence risk renal result risk of recurrence seen serum sickle cell anemia sporadic studies teratogens thalassemia tion translocation carrier trisomy trisomy 18 tumors Turner's syndrome usually X chromosome X-linked dominant X-linked recessive