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Waardenburg Syndrome Type I with Heterochromia Iridis and Circumscribed Hypopigmentation of the Skin
by
EIGELSHOVEN, SIBYLLE
,
KAMEDA, GITTA
,
KORTÜM, ANNE-KATRIN
,
HÜBSCH, SIMONE
,
ANGERSTEIN, WOLFGANG
,
SINGH, PREETI
,
VÖHRINGER, RENATE
,
GOECKE, TIMM
,
MAYATEPEK, ERTAN
,
RUZICKA, THOMAS
,
WILDHARDT, GABRIELE
,
MEISSNER, THOMAS
,
KRUSE, ROLAND
Published in
Pediatric dermatology
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Pediatric Dermatology
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Anodontia - Genetics
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Anodontia - Pathology
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Child, Preschool
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Dermatology
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Female
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Hearing Loss, Sensorineural - Genetics
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Hearing Loss, Sensorineural - Pathology
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Humans
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Hypopigmentation - Genetics
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Hypopigmentation - Pathology
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Iris Diseases - Genetics
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Iris Diseases - Pathology
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Life Sciences & Biomedicine
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Mutation, Missense
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Paired Box Transcription Factors - Genetics
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Pax3 Transcription Factor
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Pediatrics
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Science & Technology
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Waardenburg Syndrome - Genetics
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Waardenburg Syndrome - Pathology
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Wiley-Blackwell Journals
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Wiley
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