Pages that link to "Q57251199"

The following pages link to A high-density YAC contig map of human chromosome 22 (Q57251199):

Displaying 16 items.

• The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family (Q22008688) (← links)
• Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. (Q24540203) (← links)
• Genomic disorders on 22q11 (Q24563977) (← links)
• An integrated physical map for the short arm of human chromosome 5. (Q30829664) (← links)
• Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients (Q33679238) (← links)
• How is the Human Genome Project doing, and what have we learned so far? (Q33737848) (← links)
• Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11 (Q34389097) (← links)
• High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1. (Q35024299) (← links)
• Coincidence of synteny breakpoints with malignancy-related deletions on human chromosome 3. (Q35143751) (← links)
• Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. (Q35238706) (← links)
• Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation. (Q35239185) (← links)
• Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients (Q35249478) (← links)
• A bacterial artificial chromosome-based framework contig map of human chromosome 22q. (Q36806172) (← links)
• Physical mapping of the rice genome with BACs (Q36881900) (← links)
• Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region (Q43104703) (← links)
• Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23 (Q56459580) (← links)