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Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population
by
Fedick, A.M.
,
Shi, L.
,
Jalas, C.
,
Treff, N.R.
,
Ekstein, J.
,
Kornreich, R.
,
Edelmann, L.
,
Mehta, L.
,
Savage, S.A.
Published in
Clinical genetics
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Clinical Genetics
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Ashkenazi Jewish
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Base Sequence
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Carrier Screening
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Congenital Diseases
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Dna Helicases - Genetics
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Dyskeratosis Congenita
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Dyskeratosis Congenita - Diagnosis
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Dyskeratosis Congenita - Genetics
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Female
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Fetal Growth Retardation - Diagnosis
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Fetal Growth Retardation - Genetics
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Genetic Carrier Screening - Methods
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Genetic Disorders
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Genetic Testing
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Genetics & Heredity
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Germ-Line Mutation
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Haplotypes - Genetics
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Hoyeraal-Hreidarsson Syndrome
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Hoyeraal–Hreidarsson Syndrome
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Humans
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Wiley-Blackwell Journals
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Wiley
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