Additional file 2: of Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3

Autor:	F. Elli, L. DeSanctis, M.A. Maffini, P. Bordogna, D. Tessaris, A. Pirelli, M. Arosio, A. Linglart, G. Mantovani
Rok vydání:	2019
DOI:	10.6084/m9.figshare.7558058.v1
Popis:	Figure S1. 2q37 marker analysis in iPPSD3 deleted patients for confirm and characterize found structural rearrangements. Selection of homozygous (1 peak) and heterozygous (2 peaks) VNTRs from patients 3 (right panels) and 4 (left panels). (PPTX 4081 kb)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87638a00f4c5c13a5553f19904a4fa54 Zobrazit plný text záznamu