A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development

Keyphrases

• 46,XY Disorders of Sex Development 100%
• Exon Deletion 100%
• Germ Cells 66%
• Gonad Development 66%
• Genetic Counseling 33%
• Knock-in Mouse Model 33%
• Congenital Disorders 33%
• Histological Analysis 33%
• Heterozygous Deletion 33%
• Duplication 33%
• Causative mutation 33%
• Genomic DNA (gDNA) 33%
• SNP Array 33%
• Illumina 33%
• Optimal Treatment 33%
• Exon 9 33%
• Gonad 33%
• Disorders of Sex Development 33%
• At Birth 33%
• Exon 6 33%
• Exon 5 33%
• Undifferentiated Gonadal Tissue 33%
• Ambiguous Genitalia 33%
• Genital Development 33%
• Chromosome 16 33%
• CDNA Analysis 33%
• Wwox 33%
• Genome-wide SNPs 33%
• WWOX Gene 33%
• Immature Testis 33%
• Gonadal Abnormalities 33%
• Coding Sequence 33%
• Reading Frame 33%

Biochemistry, Genetics and Molecular Biology

• Exon 100%
• WWOX 100%
• Germline 25%
• Germ Cell 25%
• Mouse Model 25%
• Genetic Counseling 25%
• Single Nucleotide Polymorphism 25%
• Microarrays 25%
• Knockout Mouse 25%
• Gonad Development 25%
• Chromosome 16 25%
• Reading Frame 25%
• Genomics 25%