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American Journal of Medical Genetics|September 14, 1999
Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndromeC Sreekantaiah, D Kronn, R C Marinescu, et al.Genomics|January 1, 1995
The structural genes, MEP1A and MEP1B, for the alpha and beta subunits of the metalloendopeptidase meprin map to human chromosomes 6p and 18q, respectivelyJ S Bond, K Rojas, J Overhauser, et al.American Journal of Human Genetics|June 1, 1994
Interstitial deletions are not the main mechanism leading to 18q deletionsG Strathdee, W Harrison, H C Riethman, et al.Cytogenetics and Cell Genetics|January 1, 1997
Development of diagnostic tools for the analysis of 5p deletions using interphase FISHM Gersh, D Grady, K Rojas, et al.Genomics|August 1, 1997
Cytoplasmic antiproteinase 2 (PI8) and bomapin (PI10) map to the serpin cluster at 18q21.3A J Bartuski, Y Kamachi, C Schick, et al.Clinical Genetics|November 27, 1998
t(1;18)(q32.1;q22.1) associated with genitourinary malformationsE R Frizell, R Sutphen, F B Diamond, et al.Molecular Psychiatry|July 13, 2000
Identification of candidate genes for psychiatric disorders on 18p11K Rojas, L Liang, E I Johnson, et al.Biochemical and Biophysical Research Communications|February 17, 1998
Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate intervalA D Simmons, A W Püschel, J D McPherson, et al.AJNR. American Journal of Neuroradiology|November 1, 1996
White matter changes associated with deletions of the long arm of chromosome 18 (18q- syndrome): a dysmyelinating disorder?L A Loevner, R M Shapiro, R I Grossman, et al.Journal of Medical Genetics|February 9, 2000
5p14 deletion associated with microcephaly and seizuresE I Johnson, R C Marinescu, H H Punnett, et al.Pageof 8