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Genetic counselling in Mendelian disorders
Genetic counselling in nonMendelian disorders
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affected child affected individuals affected males amniocentesis associated autosomal dominant autosomal dominant inheritance autosomal recessive Autosomal recessive Autosomal autosomal recessive disorders autosomal recessive inheritance Birth blood cancer carrier detection cells cent Chapter childhood clinical clinicians congenital heart consanguinity couple deafness deficiency diabetes dominantly inherited Down's syndrome Duchenne muscular dystrophy dysplasia factors family members female fetal first-degree relatives follow autosomal recessive following autosomal dominant frequency gene genetic counselling genetic risks haemophilia Harper P. S. healthy heart disease hereditary heterozygotes high risk Huntington's chorea important increase isolated major malformations maternal Medical Genetics Mendelian inheritance mental retardation metabolic mutation myotonic dystrophy neural tube defects normal onset parents patients pedigree polygenic population possible pregnancy prenatal diagnosis prior risk problems rare recessive Autosomal recessive recurrence risk result risk for offspring severe situation specific spina bifida Table tests translocation tumours twin usually variable X-linked disorders X-linked recessive