Founder Effect at PGL1 in Hereditary Head and Neck Paraganglioma Families from The Netherlands
- 1 August 1998
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 63 (2), 468-473
- https://doi.org/10.1086/301951
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23Genomics, 1997
- First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).Journal of Medical Genetics, 1996
- Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23Nature Genetics, 1996
- Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequenciesCurrent Biology, 1995
- Carrier detection of Batten disease (Juvenile neuronal ceroid‐lipofuscinosis)American Journal of Medical Genetics, 1995
- The CEPH Consortium Linkage Map of Human Chromosome 11Genomics, 1995
- Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasisNature Genetics, 1994
- A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qterHuman Molecular Genetics, 1992
- Hypothyroidism and chemodectoma in father and daughter: a new syndrome of a coincidence?Clinical Endocrinology, 1992
- GENOMIC IMPRINTING IN HEREDITARY GLOMUS TUMOURS: EVIDENCE FOR NEW GENETIC THEORYThe Lancet, 1989