Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the ?critical segment? towards the telomere
- 1 March 1991
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 86 (5) , 481-483
- https://doi.org/10.1007/bf00194637
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Physical maps of 4p16.3, the area expected to contain the Huntington disease mutationGenomics, 1990
- Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeHuman Genetics, 1989
- MAPPING OF RECOMBINANTS NEAR THE HUNTINGTON DISEASE LOCUS BY USING G8 (D4S10) AND NEWLY ISOLATED MARKERS IN THE D4S10 REGION1989
- Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf–Hirschhorn syndromeNature, 1985
- The critical monosomic segment involved in 4p- syndrome: A high-resolution banding study on five inherited casesJournal of Human Genetics, 1984
- CLINICAL AND CYTOGENETIC STUDIES IN A LARGE (4-8) TRANSLOCATION FAMILY WITH PRENATAL AND POSTNATAL WOLF SYNDROME1984
- Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]Human Genetics, 1981