Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3
Open Access
- 1 September 1991
- Vol. 11 (1) , 193-198
- https://doi.org/10.1016/0888-7543(91)90118-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionGenomics, 1991
- A genetic linkage map of the human genomeCell, 1987
- Characterization of a panel of highly variable minisatellites cloned from human DNAAnnals of Human Genetics, 1987
- Mandibulofacial dysostosis (Treacher Collins syndrome): A new proposal for its pathogenesisAmerican Journal of Medical Genetics, 1987
- Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5Nucleic Acids Research, 1987
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase BHuman Genetics, 1983
- A deletion in chromosome 22 can cause digeorge syndromeHuman Genetics, 1981
- Anatomical abnormalities in mandibulofacial dysostosisAmerican Journal of Medical Genetics, 1979
- The pathogenesis of the treacher Collins syndrome (Mandibulofacial dysostosis)British Journal of Oral Surgery, 1975