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Introduction to Genetics
Bolsic Genetics 40
16 other sections not shown
affected child affected persons amniotic fluid Amyloidosis anemia anomalies approximately associated autosomal dominant autosomal dominant mode autosomal recessive autosomal recessive mode baby birth defects CARRIER DETECTION cleft lip Clin condition congenital heart congenitol couple cryptorchidism Decreased octivity diabetes disorders dominant inheritance Down's syndrome dwarfism dysplasia enzyme females fetal fetoscopy foce follows an autosomal frequently gene genetic counseling genetic disease growth deficiency Gynecol hypertelorism hypoplasia hypoplastic hypoplosio infection infoncy involves isolated defect lesions leukemia limbs lorge males malformations malignant maternal mental retardation metabolic microcephaly micrognothid mild mode of inheritance Multiple muscle muscular dystrophy nasal bridge normal Obstet occosional occur omniotic fluid cells onset ovdiloble palate parents Pediatr phenotype pregnancy prenatal diagnosis Prenatol refordation renal retardotion seen serum severe sickle cell skin Smoll specific studies teratogens thalassemia tissue translocation trisomy trisomy 13 tumors Turner's syndrome usually USudly Sporodic X chromosome X-linked recessive