
Mosaic trisomy 15 | About the Disease | GARD - Genetic and Rare ...
Mosaic trisomy 15 is a rare chromosomal anomaly syndrome principally characterized by intrauterine growth restriction, congenital cardiac anomalies (incl. ventricular and atrial septal …
Chromosome 15, Distal Trisomy 15q - NORD
2009年4月10日 · Chromosome 15, Distal Trisomy 15q is an extremely rare chromosomal disorder in which the end (distal) portion of the long arm (q) of the 15th chromosome appears three …
Chromosome 15, Distal Trisomy 15q - Kaiser Permanente
2009年4月10日 · Chromosome 15, Distal Trisomy 15q is an extremely rare chromosomal disorder in which the end (distal) portion of the long arm (q) of the 15th chromosome (15q) appears …
Understanding Chromosome 15 Disorders: A High-Level Guide
Chromosome 15 disorders encompass a range of genetic conditions that result from deletions, duplications or other mutations within the genes located on this specific chromosome. These …
Orphanet: Mosaic trisomy 15 syndrome
Mosaic trisomy 15 is a rare chromosomal anomaly syndrome principally characterized by intrauterine growth restriction, congenital cardiac anomalies (incl. ventricular and atrial septal …
15号染色体三体、嵌合体及单亲二体的产前遗传学诊断及临床特征
15 号染色体三体( trisomy 15 , T15 ) , 简称 15-三体 , 常由于生殖细胞减数分裂或细胞分裂后期染色体不分离引起。 15- 三体常导致胚胎停育或胎儿多发畸形而流产; 15- 三体嵌合体可 …
mosaic trisomy 15 - National Organization for Rare Disorders
Mosaic trisomy 15 is a rare chromosomal anomaly syndrome principally characterized by intrauterine growth restriction, congenital cardiac anomalies (incl. ventricular and atrial septal …
Mosaic trisomy 15 - NIH Genetic Testing Registry (GTR) - NCBI
Clinical resource with information about Mosaic trisomy 15 and its clinical features, available genetic tests from US and labs around the world and links to practice guidelines and …
15号染色体及相关疾病 - 360doc
UPD机制: 三体自救(trisomy rescue): 减数分裂出现错误的精子(卵子)和卵子(精子)结合形成15号染色体三体受精卵,在胚胎早期有丝分裂过程中失去一条染色体。
Trisomy 15 (Concept Id: C0795856) - National Center for …
Trisomy 15 is frequently observed as a minor clone in patients with Anemia/MDS/NHL and as a major clone in patients with AML.
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