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Genetic haploinsufficiency as a phenotypic determinant of a deletion 13q syndrome
by
Kasyan
,
Armen G
,
Benirschke, Kurt
Published in
Pediatric and developmental pathology
(01.11.2005)
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Journal Article
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medicine
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abnormalities, multiple - genetics
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abnormalities, multiple - pathology
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brain - abnormalities
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chromosome aberrations
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chromosome deletion
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chromosomes, human, pair 13 - genetics
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English
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