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2006, Genetic syndromes and communication disorders series, ISBN 1597560219, xiv, 136
Book
Journal of medical genetics, ISSN 0022-2593, 08/1997, Volume 34, Issue 8, pp. 656 - 665
Auditory-pigmentary syndromes are caused by physical absence of melanocytes from the skin, hair, eyes, or the stria vascularis of the cochlea. Dominantly... 
Eye Color | Waardenburg Syndrome - epidemiology | Prevalence | Receptors, Endothelin - genetics | Face - pathology | Humans | Endothelin-3 - genetics | Male | Waardenburg Syndrome - pathology | Incidence | Homozygote | Waardenburg Syndrome - genetics | Female
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/1997, Volume 34, Issue 8, pp. 656 - 665
Auditory-pigmentary syndromes are caused by physical absence of melanocytes from the skin, hair, eyes, or the stria vascularis of the cochlea. Dominantly... 
Waardenburg syndrome | Auditory-pigmentary syndromes | MICROPHTHALMIA GENE | INNER-EAR | HUP2 PAIRED DOMAIN | DOMINANT INHERITANCE | K KM GENETICS & HEREDITY | SPLOTCH MOUSE | auditory-pigmentary syndromes | SYNDROME TYPE-I | GENETICS & HEREDITY | HIRSCHSPRUNG-DISEASE | MUTATIONS | HUMAN HOMOLOG | PAX-GENES
Journal Article
Case Reports- Waardenburg syndrome type 2 in an African patient, 12/2005
A thirty six year-old African man, born in the Southern part of Libya, presented with congenital deafness and white forelock, variable-sized hypopigmented,... 
Waardenburg syndrome type 2, White forelock, Bilateral iris hypochromia
Journal
PLoS genetics, ISSN 1553-7390, 2011, Volume 7, Issue 7, p. e1002114
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2017, Volume 173, Issue 4, pp. 1066 - 1070
Diagnosis of genetic syndromes may be difficult when specific components of a disorder manifest at a later age. We present a follow up of a previous report... 
central demyelinating leukodystrophy | WS4 | peripheral demyelinating neuropathy | Waardenburg syndrome | Waardenburg–Shah syndrome | 22q duplication syndrome | DAX1 | DOMINANT | DELETION | Waardenburg-Shah syndrome | GENETICS & HEREDITY | CHROMOSOME-22 | MICE | MUTATIONS | SRY | Chromosome Duplication | Demyelinating Diseases - genetics | Humans | Hirschsprung Disease - genetics | African Americans | Male | Kidney Failure, Chronic - ethnology | Pelizaeus-Merzbacher Disease - ethnology | Waardenburg Syndrome - ethnology | Demyelinating Diseases - diagnosis | Kidney Failure, Chronic - pathology | Pelizaeus-Merzbacher Disease - pathology | Demyelinating Diseases - pathology | Hirschsprung Disease - ethnology | Chromosomes, Human, Pair 22 - chemistry | Kidney Failure, Chronic - diagnosis | Pelizaeus-Merzbacher Disease - genetics | Hirschsprung Disease - pathology | Waardenburg Syndrome - pathology | Pelizaeus-Merzbacher Disease - diagnosis | Kidney Failure, Chronic - genetics | Hirschsprung Disease - diagnosis | Waardenburg Syndrome - diagnosis | Demyelinating Diseases - ethnology | Waardenburg Syndrome - genetics | 46, XX Testicular Disorders of Sex Development | SOXE Transcription Factors - genetics | Hirschsprung's disease | Analysis | DNA microarrays | Genes | Index Medicus | PCWH | Sex reversal | and Hirschsprung disease | 22q11 duplication syndrome | neurocristopathies | SOX10 | XX male syndrome | disorders of sex development
Journal Article
Journal Article
Medical Journal Armed Forces India, ISSN 0377-1237, 10/2018, Volume 74, Issue 4, pp. 380 - 382
Journal Article
PIGMENT CELL & MELANOMA RESEARCH, ISSN 1755-1471, 01/2013, Volume 26, Issue 1, pp. 78 - 87
Journal Article