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Tests By Disease/Condition
Anencephaly
Bloom Syndrome
Canavan Disease
Chromosome Abnormalities
Cystic Fibrosis
Down Syndrome
Familial Dysautonomia
Fanconi Anemia Group C
Fragile X Syndrome
Gaucher Disease
Glycogen Storage Disease Type 1A
Inherited Diseases (when specific risks have been identified)
Maple Syrup Urine Disease
Mucolipidosis Type IV
Niemann-Pick Disease Type A
Open Neural Tube Defects
Sickle Cell Disease
Spina Bifida
Spinal Muscular Atrophy
Tay-Sachs Disease
Trisomy 13
Trisomy 18
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