Experience of carrier couples identified through a population-based carrier screening pilot program for four founder autosomal recessive diseases in Saguenay-Lac-Saint-Jean. [electronic resource]
Producer: 20181114Description: 67-74 p. digitalISSN:- 1097-0223
- Adult
- Agenesis of Corpus Callosum -- diagnosis
- Cytochrome-c Oxidase Deficiency -- diagnosis
- Female
- Founder Effect
- Genetic Carrier Screening
- Heterozygote
- Humans
- Leigh Disease -- diagnosis
- Male
- Muscle Spasticity -- diagnosis
- Peripheral Nervous System Diseases -- diagnosis
- Pilot Projects
- Spinocerebellar Ataxias -- congenital
- Tyrosinemias -- diagnosis
- Young Adult
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Publication Type: Journal Article
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