Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern

• المؤلفون الرئيسيون: Tan, E.-S, Yong, M.-H, Lim, E.C.P, Li, Z.-H, Brett, M.S.Y, Tan, E.-C
• مؤلفون آخرون: INSTITUTE OF MOLECULAR & CELL BIOLOGY
• التنسيق: مقال
• منشور في: 2020
• الموضوعات: polypeptide; small nuclear ribonucleoprotein; array comparative genomic hybridization; article; autism; case report; cell population; chromosome 15q; chromosome 15q11; chromosome 15q12; chromosome 15q13; chromosome analysis; comparative genomic hybridization; developmental disorder; DNA microarray; female; fluorescence in situ hybridization; gene; gene dosage; genetic disorder; human; human cell; male; marker chromosome; methylation; muscle hypotonia; neurologic disease; phenotype; priority journal
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/181756

10.1186/1755-8166-7-32