Interstitial deletion of chromosome 15: two cases
- 1 December 1988
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 80 (4) , 401-404
- https://doi.org/10.1007/bf00273663
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Ring chromosome 15 syndrome. Further delineation of the adult phenotype.1986
- del(15)(q22q24) Syndrome with Potter sequenceAmerican Journal of Medical Genetics, 1984
- Cytogenetic studies of familial Prader-Willi syndromeHuman Genetics, 1984
- INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 151982
- Localization of MPI, PKM2, IDHM, and the α subunit of hexosaminidase (HEXA) to the q21→qter region of human chromosome 15Cytogenetic and Genome Research, 1978
- Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and β2 microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrierCytogenetic and Genome Research, 1978
- Assignment of the structural genes for the ? subunit of hexosaminidase A, mannosephosphate isomerase, and pyruvate kinase to the region q22-qter of human chromosome 15Somatic Cell and Molecular Genetics, 1977
- Assignment of the human genes for mannose phosphate isomerase, pyruvate kinase (M2), and hexosaminidase-A to chromosome 15Cytogenetic and Genome Research, 1976
- Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13Annals of Human Genetics, 1975