FMR1 gene deletion/reversion: a pitfall of fragile X carrier testing

scientific article published in January 2003

FMR1 gene deletion/reversion: a pitfall of fragile X carrier testing is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/109065703322783653
P698PubMed publication ID15000806

P50authorFrank KooyQ37843120
P2093author name stringHolinski-Feder E
Gasteiger M
Grasbon-Frodl E
Neitzel B
P433issue4
P304page(s)303-308
P577publication date2003-01-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleFMR1 gene deletion/reversion: a pitfall of fragile X carrier testing
P478volume7

Reverse relations

cites work (P2860)
Q36338209EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders
Q36050548Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions
Q81083809Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature
Q36302118Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders
Q27011565Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders
Q89944369Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families

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