Regional mapping panel for human chromosome 17: Application to neurofibromatosis type 1
- 31 December 1987
- Vol. 1 (4) , 374-381
- https://doi.org/10.1016/0888-7543(87)90042-5
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Tightly linked markers for the neurofibromatosis type 1 geneGenomics, 1987
- Cases of neurofibromatosis with rearrangements of chromosome 17 involving band 17q11.2American Journal of Medical Genetics, 1987
- Interstitial deletion of (17)(p11.2p11.2): Report of six additional patients with a new chromosome deletion syndromeAmerican Journal of Medical Genetics, 1986
- Interstitial deletion of (17)(p11.2p11.2) in nine patientsAmerican Journal of Medical Genetics, 1986
- The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2Biochemical and Biophysical Research Communications, 1985
- Localization of the oncogene c‐erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17Annals of Human Genetics, 1985
- Unbalanced translocation (15;17)(q13;p13.3) with apparent Prader‐Willi syndrome but without Miller‐Dieker syndromeAmerican Journal of Medical Genetics, 1985
- Miller-Dieker syndrome: Lissencephaly andmonosomy 17pThe Journal of Pediatrics, 1983
- Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22Nature, 1974
- Regional Localization of the Human Genes for Thymidine Kinase, Lactate Dehydrogenase-A, and Esterase-A4Cytogenetic and Genome Research, 1974