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Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis
by
Rothnagel, Joseph A.
,
Lin, Michael T. S.
,
Longley, Mary A.
,
Holder, Rhanda A.
,
Hazen, Paul G.
,
Levy, Moise L.
,
Roop, Dennis R.
Published in
Prenatal diagnosis
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Peer Reviewed
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Articles
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Journal Title
Prenatal Diagnosis
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Subjects
Amniotic Fluid - Cytology
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Biological And Medical Sciences
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Disease
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Dna Mutational Analysis
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Dna Restriction Enzymes
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Female
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Genetics
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Genetics & Heredity
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Gynecology. Andrology. Obstetrics
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Humans
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Hyperkeratosis, Epidermolytic - Diagnosis
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Hyperkeratosis, Epidermolytic - Genetics
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Intermediate Filaments
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Keratins - Genetics
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Life Sciences & Biomedicine
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Management. Prenatal Diagnosis
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Medical Sciences
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Mosaicism
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Mutation
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Obstetrics & Gynecology
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1400 : 2026
1400
2026
Source
Wiley-Blackwell Journals (Backfile Content)
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Wiley
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