Orphanet Journal of Rare Diseases BioMed Central

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NSD1 Weaver syndrome Overgrowth syndrome DiGeorge syndrome Perlman syndrome Chromosome 5 Beckwith–Wiedemann syndrome Dolichocephaly Health Syndromes Sotos syndrome		Orphanet Journal of Rare Diseases BioMed Central Add to Reading List Source URL: www.ojrd.com Download Document from Source Website File Size: 269,25 KB Share Document on Facebook

	RIMD–IPR Joint Seminar “Insight into the functions of the CRK gene family from a view of DiGeorge Syndrome” Akira Imamoto D.D.S., Ph.D. The University of Chicago DocID: 1vjjV - View Document
	® What is NACE Plus ? NACE Plus® has the same characteristics as the NACE® test , but is an extended version that also incorporates the detection of chromosome 9 and 16 trisomies, which are closely related with DocID: 1pXed - View Document
	Clinical and Molecular Cytogenetics Laboratory DEPARTMENT OF PATHOLOGY UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER, SAN ANTONIO CLIA# 45D0660483 CAP# Room 318C, 7703 Floyd Curl Drive, San Antonio, TXPho DocID: 1p62J - View Document
	ECHO Adult study  ECHO study is a research group based at Cardiff University that wants to find out more about the life course and health of individuals with genetic syndromes. We are currently looking to hear from ad DocID: 1onbS - View Document
	ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop DocID: 1ahHZ - View Document