The Gene for Naegeli–Franceschetti–Jadassohn Syndrome Maps to 17q21
- 1 October 2000
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 115 (4) , 694-698
- https://doi.org/10.1046/j.1523-1747.2000.00097.x
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Construction of a Detailed Physical and Transcript Map of the FTDP-17 Candidate Region on Chromosome 17q21Genomics, 1999
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in RecombinationAmerican Journal of Human Genetics, 1998
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Mutation of a type II keratin gene (K6a) in pachyonychia congenitaNature Genetics, 1995
- Isolation of a diverged homeobox gene, M0X1, from the BRCA1 region on 17q21 by solution hybrid captureHuman Molecular Genetics, 1994
- A novel metalloprotease/disintegrin–like gene at 17q21.3 is somatically rearranged in two primary breast cancersNature Genetics, 1993
- The Nägeli-Franceschetti-Jadassohn Syndrome: A Hereditary Ectodermal Defect Leading to Colloid-Amyloid Formation in the DermisDermatology, 1993
- Structure and chromosomal location of the human granulin geneBiochemical and Biophysical Research Communications, 1992
- Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains.Proceedings of the National Academy of Sciences, 1992
- A propos de l’«Incontinentia pigmenti», délimitation de deux syndromes différents figurant sous le même termeDermatology, 1954