Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization

Author:

Chen Chih-Ping,Kuo Yung-Ting,Lin Shuan-Pei,Su Yi-Ning,Chen Yann-Jang,Hsueh Rui-Yuan,Lin Yi-Hui,Wu Pei-Chen,Lee Chen-Chi,Chen Yu-Ting,Wang Wayseen

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference29 articles.

1. Molecular analysis of the 18q-syndrome and correlation with phenotype;Kline;Am J Hum Genet,1993

2. The 18q-syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2;Silverman;Am J Hum Genet,1995

3. Analysis of clinical variation seen in patients with 18q terminal deletions;Strathdee;Am J Med Genet,1995

4. Délétion partielle du bras long du chromosome 18;de Grouchy;Pathol Biol,1964

5. Chromosome 18, monosomy 18q;Greenberg,1990

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