id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
cajgh-336	Vaiman, Michael; Shilco, Phillip; Roitblat, Yulia; Padilla-Raygoza, Nicolas; Leit, Aidan; Kavin, Aaron; Schonberger, Edan; Nehuliaieva, Liliia; Buchris, Noa; Shterenshis, Michael	Screening Procedure for Hemihypertrophy: Preliminary Results of International Multicenter Prospective Study	2019	7	.pdf	application/pdf	3230	165	35	While numerous reports on genetic abnormalities in IH cases were published, additional assessment of other family members to rule out any kind of body asymmetry may be highly informative because hereditary basis of the disorder, the instability of the 11p15.5 chromosomal region, is very well established.1-5,8-10 A close connection between IH and Wilms tumor (nephroblastoma, a common pediatric neoplasm of the kidney) was postulated already in the 1950s and was confirmed in more recent Conclusion: We present an easy-to-use selection tool to identify children with suspected IH, which results in the selection of the risk group that may benefit from referral to a pediatrician and a clinical geneticist.	cache/cajgh-336.pdf	txt/cajgh-336.txt