Identification of Cryptic Rearrangements in Patients with 18q− Deletion Syndrome
- 1 June 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (6) , 1500-1506
- https://doi.org/10.1086/301854
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Preliminary definition of a “critical region” of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literatureAmerican Journal of Medical Genetics, 1993
- Recognizable behavioral and somatic phenotype in patients with proximal interstitial 18q deletion: Report on a new affected child and follow‐up on the original reported familial casesAmerican Journal of Medical Genetics, 1992
- Monosomy 18q 12.1→21.1: A recognizable aneuploidy syndrome? Report of a patient and review of the literatureAmerican Journal of Medical Genetics, 1992
- Neurologic manifestations in 18q– syndromeAmerican Journal of Medical Genetics, 1990
- Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.Proceedings of the National Academy of Sciences, 1990
- Use of cyclosporin a in establishing epstein-barr virus-transformed human lymphoblastoid cell linesIn Vitro Cellular & Developmental Biology - Plant, 1984
- Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome bandingCytogenetic and Genome Research, 1984
- Polymorphic DNA region adjacent to the 5' end of the human insulin gene.Proceedings of the National Academy of Sciences, 1981
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960