13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size...

medical syndromes. 1p36 deletion syndrome 1q21.1 deletion syndrome 1q21.1 duplication syndrome 13q deletion syndrome 17q21.31 microdeletion syndrome 22q11...

Lange syndrome Orofaciodigital syndrome 1 13q deletion syndrome XXYY syndrome Silver–Russell syndrome Andersen-Tawil syndrome Noonan syndrome Ehlers–Danlos...

Patau syndrome, mosaic trisomy 9, 13q deletion syndrome, Wolf–Hirschhorn syndrome) or monogenetic Mendelian disorders (e.g. CHARGE syndrome, Fraser...

(2009). "Clinical variability of Waardenburg–Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus". American...

syndrome, short rib–polydactyly syndrome type 1, Townes–Brocks syndrome, 13q deletion syndrome, urorectal septum malformation sequence and the OEIS complex...

Chromosome 13q deletion Chromosome 13q trisomy Chromosome 13q-mosaicism Chromosome 14 ring Chromosome 14 trisomy Chromosome 14, deletion 14q, partial...

disorders are some of those related to genes on chromosome 13: 13q deletion syndrome Bipolar disorder Bladder cancer Breast cancer Heterochromia Hirschsprung's...

smoking, previous chemotherapy or radiation therapy, myelodysplastic syndrome, and exposure to the chemical benzene. The underlying mechanism involves...

as chronic lymphocytic leukemia. Cri du Chat (CdC) is a syndrome caused by a partial deletion of the short arm of chromosome 5. Several studies have shown...

of 8–10 years; deletion of chromosome 13q is associated with a median OS of 17 years; and trisomy of chromosome 12, as well as deletion of chromosome 11q...

tract). Radiation exposure Somatic mutation, such as deletion of chromosome 9q, 9p, 11p, 17p, 13q, 14q and overexpression of RAS (oncogene) and epidermal...

carcinoma, hereditary leiomyomatosis, Birt–Hogg–Dube syndrome, hyperparathyroidism-jaw tumor syndrome, familial papillary thyroid carcinoma, von Hippel–Lindau...

genetic findings that may be associated with poor outcomes include: 13q deletion, 7q gain, ID3 and CCND3 double-hit mutations, and 18q21 CN-LOH mutations...

Abeliovich D (November 2001). "A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation...

cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere". American Journal of Human Genetics. 66...