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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 and location of the deletion on chromosome 13 , the physical and mental manifestations will vary.
Other chromosomal conditions: Partial monosomy 13q is a rare chromosomal disorder that results when a piece of the long arm (q) of chromosome 13 is missing (monosomic). Infants born with partial monosomy 13q may exhibit low birth weight, malformations of the head and face (craniofacial region), skeletal abnormalities (especially of the hands ...
Partial monosomy of chromosome 13q is a monosomy that results from the loss of all or part of the long arm of chromosome 13 in human beings. It is a rare genetic disorder which results in severe congenital abnormalities which are frequently fatal at an early age.
13q deletion syndrome; 17q21.31 microdeletion syndrome; 22q11.2 distal deletion syndrome; 22q11.2 duplication syndrome; 22q13 deletion syndrome; 2p15-16.1 microdeletion syndrome; 2q37 deletion syndrome; 3-M syndrome; 3C syndrome; 3q29 microdeletion syndrome; 49,XXXXY; 4D syndrome; 8p23.1 duplication syndrome; 9q34 deletion syndrome
13q deletion syndrome; C. Cleft palate short stature vertebral anomalies syndrome; Corneodermatoosseous syndrome; F. Fine–Lubinsky syndrome; H. Hand and foot ...
1p36 deletion syndrome; 1q21.1 duplication syndrome; 2p15-16.1 microdeletion syndrome; 2q37 deletion syndrome; 3-M syndrome; 3C syndrome; 3q29 microdeletion syndrome; 8p23.1 duplication syndrome; 9q34.3 deletion syndrome; 13q deletion syndrome; 15q overgrowth syndrome
Chromosomal deletion syndromes result from deletion of parts of chromosomes. Depending on the location, size, and whom the deletion is inherited from, there are a few known different variations of chromosome deletions. Chromosomal deletion syndromes typically involve larger deletions that are visible using karyotyping techniques.
13q deletion syndrome; T. Toriello–Carey syndrome This page was last edited on 30 October 2017, at 17:37 (UTC). Text is available under the Creative Commons ...