Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B
- 1 September 1983
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 64 (3) , 305-308
- https://doi.org/10.1007/bf00279420
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The role of position in determining homoeotic gene function in DrosophilaNature, 1982
- Familial pericentric inversion of chromosome 1 in a boy with Goldenhar's syndromeHuman Genetics, 1982
- Abnormal phenotype in a child with the same balanced translocation (5;7)(p15;q22) as his fatherClinical Genetics, 1981
- Major rearrangement in the human β-globin gene clusterNature, 1981
- DUCHENNE MUSCULAR-DYSTROPHY (DMD) IN A FEMALE WITH AN X-AUTOSOME TRANSLOCATION - FURTHER EVIDENCE THAT THE DMD LOCUS IS AT XP211981
- Evidence for a Null allele at the Esterase D (EC 3.1.1.1) locusHuman Genetics, 1979
- Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parentsHuman Genetics, 1979
- Are balanced translocations really balanced? Preliminary cytogenetic evidence for position effect in man.1978
- A cytogenetic survey of 14,069 newborn infantsClinical Genetics, 1975
- Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).1975