id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_45exwtryazgfvgtelrby5jmywa	Rossella Bruno	A 17q duplication prenatally detected	2015.0	4	.pdf	application/pdf	1894	247	36	chromosome 17q detected in prenatal diagnosis. prenatally; postnatal cases with a similar chromosomal anomaly subtelomeric regions showed two normal signals (Fig. 4), confirming array-CGH data. Partial 17q duplication is a rare anomaly, and most of the patients reported in literature have undergone postnatal analysis Karyotype shows a duplication of the long arm of chromosome 17. Most cases of partial trisomy for the distal region of 17q are due Array-comparative genomic hybridization profile of the duplicated region. parative genomic hybridization showing the presence of a duplication of chromosome OMIM genes located in the duplicated region 17q23-25. OMIM genes located in the duplicated region 17q23-25. Duplication of 17q region as sole chromosome anomaly reported in literature and in The authors have no conflicts of interest relevant to this article. diagnosis of mosaicism for partial trisomy 8: a case report including fetal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q.	./cache/work_45exwtryazgfvgtelrby5jmywa.pdf	./txt/work_45exwtryazgfvgtelrby5jmywa.txt