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Volumn 44, Issue 4, 2007, Pages
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Hypomethylation in the 11p15 telomeric imprinting domain in a patient with Silver-Russell syndrome with a CSH1 deletion (17q24) renders a functional role of this alteration unlikely.
a a a a
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Author keywords
[No Author keywords available]
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Indexed keywords
PLACENTA LACTOGEN;
CHROMOSOME 17;
CHROMOSOME DELETION;
CHROMOSOME MAP;
DNA METHYLATION;
GENETIC EPIGENESIS;
GENETICS;
GENOME IMPRINTING;
HUMAN;
LETTER;
MULTIPLE MALFORMATION SYNDROME;
PHYSIOLOGY;
SOUTHERN BLOTTING;
SYNDROME;
TELOMERE;
ULTRASTRUCTURE;
ABNORMALITIES, MULTIPLE;
BLOTTING, SOUTHERN;
CHROMOSOME DELETION;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 17;
DNA METHYLATION;
EPIGENESIS, GENETIC;
GENOMIC IMPRINTING;
HUMANS;
PLACENTAL LACTOGEN;
SYNDROME;
TELOMERE;
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EID: 34248361206
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.2007.049130 Document Type: Letter |
Times cited : (6)
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References (0)
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