2q37 monosomy - definição. O que é 2q37 monosomy. Significado, conceito
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O que (quem) é 2q37 monosomy - definição


2q37 monosomy         
DELETION 2Q37 OR MONOSOMY 2Q37 IS A CHROMOSOMAL ANOMALY INVOLVING DELETION OF CHROMOSOME BAND 2Q37 AND MANIFESTS AS THREE MAJOR CLINICAL FINDINGS: DEVELOPMENTAL DELAY, SKELETAL MALFORMATIONS AND FACIAL DYSMORPHISM
Chromosome 2, monosomy 2q37
2q37 monosomy is a rare genetic disorder caused by a deletion of a segment at the end of chromosome 2.
Monosomy 9p         
HUMAN DISEASE
Monosomy 9p-
Monosomy 9p (also known as Alfi's Syndrome or simply 9P-) is a rare chromosomal disorder in which some DNA is missing or has been deleted on the short arm region, “p”, of one of the 9th Chromosomes (9p22.2-p23).
18p-         
HUMAN DISEASE
Partial monosomy 18p; De Grouchy syndrome, type 1; Monosomy 18p; 18p- syndrome
18p- is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 50,000 births.