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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1994-3-10
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pubmed:abstractText |
It is well known that the persistence of alterations in the normal embryological development of branchial arches can lead to preauricular and cervical fistulas within a family. However, until 1970, there were no reports of dysplasia affecting the branchial, otic, and renal systems (BOR syndrome) with dominant autosomic inheritance. The authors report on a family with BOR syndrome of different expressivity in three generations, and describe an unusual case of bilateral fistulas of the first and second branchial arches in a newborn.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-3468
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1527-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:8301480-Abnormalities, Multiple,
pubmed-meshheading:8301480-Branchioma,
pubmed-meshheading:8301480-Deafness,
pubmed-meshheading:8301480-Ear,
pubmed-meshheading:8301480-Female,
pubmed-meshheading:8301480-Genes, Dominant,
pubmed-meshheading:8301480-Head and Neck Neoplasms,
pubmed-meshheading:8301480-Humans,
pubmed-meshheading:8301480-Incidence,
pubmed-meshheading:8301480-Infant, Newborn,
pubmed-meshheading:8301480-Kidney,
pubmed-meshheading:8301480-Male,
pubmed-meshheading:8301480-Pedigree,
pubmed-meshheading:8301480-Syndrome
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pubmed:year |
1993
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pubmed:articleTitle |
Branchio-oto-renal syndrome: incidence in three generations of a family.
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pubmed:affiliation |
Service of Pediatric Surgery, Virgen del Camino Hospital, Pamplona, Spain.
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pubmed:publicationType |
Journal Article,
Case Reports
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