Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome
- 1 May 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (5) , 1200-1212
- https://doi.org/10.1086/375179
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Monosomy 1p36 ??? a recently delineated, clinically recognizable syndromeClinical Dysmorphology, 2002
- Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion SyndromeEpilepsia, 2001
- TUMOR SUPPRESSOR GENES ON THE SHORT ARM OF CHROMOSOME 1 IN NEUROBLASTOMAPediatric Hematology and Oncology, 2001
- The Promise and Pitfalls of Telomere Region–Specific ProbesAmerican Journal of Human Genetics, 2000
- The Promise and Pitfalls of Telomere Region–Specific ProbesAmerican Journal of Human Genetics, 2000
- Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndromeNature Genetics, 1997
- Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated SyndromeAmerican Journal of Human Genetics, 1997
- Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domainsHuman Molecular Genetics, 1997
- Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.Journal of Medical Genetics, 1995
- Genetic syndromes and uniparental disomy: A study of 16 cases of Brachmann‐de Lange syndromeAmerican Journal of Medical Genetics, 1993