|
rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
5
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|
pubmed:dateCreated |
1994-1-25
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|
pubmed:abstractText |
Chromosome analysis of a male infant and his mother with Saethre-Chotzen syndrome demonstrated an apparently balanced translocation, t(2;7)(p23;p22). This association lends support to localization of the gene for Saethre-Chotzen syndrome to the 7p2 region and supports further involvement of gene(s) in the 7p22 region.
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pubmed:grant |
|
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0148-7299
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
47
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
637-9
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pubmed:dateRevised |
2007-11-14
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|
pubmed:meshHeading |
pubmed-meshheading:8266989-Acrocephalosyndactylia,
pubmed-meshheading:8266989-Adult,
pubmed-meshheading:8266989-Chromosome Mapping,
pubmed-meshheading:8266989-Chromosomes, Human, Pair 2,
pubmed-meshheading:8266989-Chromosomes, Human, Pair 7,
pubmed-meshheading:8266989-Female,
pubmed-meshheading:8266989-Humans,
pubmed-meshheading:8266989-Infant,
pubmed-meshheading:8266989-Karyotyping,
pubmed-meshheading:8266989-Male,
pubmed-meshheading:8266989-Translocation, Genetic
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|
pubmed:year |
1993
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|
pubmed:articleTitle |
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22.
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|
pubmed:affiliation |
Division of Pediatric Genetics, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Camden.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|
