Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. [electronic resource]

By:

Salimy, Zeinab

Contributor(s):

Akbari, Mohammad Taghi
Deilamani, Faravareh Khordadpoor

Producer: 20201013ISSN:

0973-7731

Subject(s):

Alleles
Female
Fragile X Mental Retardation Protein -- genetics
Fragile X Syndrome -- diagnosis
Genetic Association Studies
Genetic Predisposition to Disease
Humans
Intellectual Disability -- diagnosis
Male
Multilocus Sequence Typing
Primary Ovarian Insufficiency -- diagnosis
Trinucleotide Repeats

In: Journal of genetics vol. 99

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Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency.

APA

Salimy Z., Akbari M. T. & Deilamani F. K. (20201013). Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. : Journal of genetics.

Chicago

Salimy Zeinab, Akbari Mohammad Taghi and Deilamani Faravareh Khordadpoor. 20201013. Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. : Journal of genetics.

Harvard

Salimy Z., Akbari M. T. and Deilamani F. K. (20201013). Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. : Journal of genetics.

MLA

Salimy Zeinab, Akbari Mohammad Taghi and Deilamani Faravareh Khordadpoor. Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. : Journal of genetics. 20201013.

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