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93 Cards in this Set
- Front
- Back
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inheritance of cystic fibrosis
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autosomal recessive
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sickle cell anemia
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autosomal recessive
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tay-saches
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autosomal recessive
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phenylketouria
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autosomal recessive
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hurler syndrome
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autosomal recessive
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xeroderma pigmentosum
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autosomal recessive
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alpha thalisemias
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autosomal dominant
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beta thalisemias
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autosomal dominant
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marfans syndrome
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autosomal dominant
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familial hypercholesterolemia
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autosomal dominant
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myotonic muscular dystophy
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autosomal dominant
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achondroplasia
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autosomal dominant
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hutchinson-gilford progeria
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autosomal dominant
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retinoblastoma
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autosomal dominant
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neurofibromatosis type 1
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autosomal dominant
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neurofibromatosis type II
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autosomal dominant
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neuroblastoma
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gene amplification
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red-green color blindness
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x linked recessive
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hemophilia a
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x linked recessive
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hemophilia b
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x linked recessive
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duchenne muscular dystrophy
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x linked recessive
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glucose 6 phosphate dehydrogenase deficiency
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x linked recessive
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lesch-nyhan syndrome
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x linked recessive
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fragile x syndrome
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x linked dominant
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severe combined immuno-deficiency syndrome
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autosomal recessive
x linked recessive |
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osteogenesis imperfecta
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autosomal recessive
autosomal dominant |
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ehlers danlos syndromes
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autosomal dominant
autosomal recessive x linked recessive |
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charcot marie tooth disease
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autosomal dominant
autosomal recessive x linked recessive x linked dominant |
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familial parkinson disease
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autosomal recessive
autosomal dominant |
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idoiopathic parkinson disease
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multifactorial
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alzhemers
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multifactorial
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diabetes mellitus
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multifactorial
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systemic lupus
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multifactorial
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leber optic neuropathy
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mitochondrial
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kearn sayre syndrome
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mitochondrial
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tripoidy
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euploidy
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down syndrome
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aneuploidy
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edwards syndrom
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aneuploidy
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patau syndrome
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aneuploidy
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turner syndrome
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aneuploidy
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klinefelter syndrome
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aneuploidy
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47 XYY syndrome
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aneuploidy
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47 XXX syndrome
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aneuploidy
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cri du chat
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aberration
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chronic myelogenous leukemia
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aberration
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burkitt lymphoma
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aberration
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46 XY females
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aberration
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46 XX males
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aberration
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prader - willi syndrome
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microdeletion
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angelman syndrome
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microdeletion
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digeorge syndrome
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microdeletion
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williams syndorme
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microdeletion
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true hermaphrodites
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aberations or chimeras
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congenital adrenal hyperplasia
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autosomal recessive
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testicular feminization syndrome
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x linked recessive
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androgen insensitivity syndrome
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x linked recessive
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cystic fibrosis
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pleiotropic heterogenetiy
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sickle cell anemia
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point mutation
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tay-sachs
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autosomal recessive
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phenylketonuria
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pleiotropic
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hurler syndrome
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pleiotropic
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xeroderma pigmentosum
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heterogeneity
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alpha thalissemias
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heterogeneity
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beta thalisemias
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heterogeneity
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marfan syndrome
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pleiotropic
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myotonic muscular dystrophy
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anticipation
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huntington disease
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anticipation
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achondroplasia
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pleiotropic
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hutchinson-gilford progeria
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autosomal dominant
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retinoblastoma
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tumor suppressor
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neurofibromatosis type I
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pleiotropic tumor suppressor
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neurofibromatosis type II
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pleiotropic tumor suppressor
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nuroblastoma
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homogeneous staining region
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hemophilia a
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heterogeneity
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hemophilia B
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heterogeneity
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fragile x syndrome
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anticipation
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SCIDS
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heterogeneity
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osteogenesis imperfecta
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heterogeneity (types I-IV)
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ehlers danlos syndromes
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heterogeneity (types I-X)
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charcot marie tooth disease
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heterogeneity sex influenced
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familial parkinson disease
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heterogeneity
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diabetes mellitus
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autoimmune
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systemic lupus
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autoimmune
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leber optic neuropathy
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hterogeneity; sex influenced
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kearn sayre syndrome
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duplication deletion
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cri du chat
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deletion of 5 p
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chronic myelogeneous Leukemia (CML)
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translocation
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burkitt lymphoma
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translocation
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46 XY females
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deletion (X)
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46 XX Males
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insertion (Y)
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prader -willi syndrome
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epigenetic imprinting
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angelman syndrome
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epigenetic imprinting
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true hermaphrodites
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translocation or embryonic fusions
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