De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
Author:
Affiliation:
1. Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U-393, Hôpital des Enfants-Malades, Paris, France.
2. Genethon, Evry, France.
3. Centre d'Etudes du Polymorphisme Humain (CEPH), Paris, France.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference20 articles.
1. BRZUSTOWICZ, L.M., GENETIC-MAPPING OF CHRONIC CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY TO CHROMOSOME-5Q11.2-13.3, NATURE 344: 540 (1990).
2. CHUMAKOV, I.M., ISOLATION OF CHROMOSOME-21-SPECIFIC YEAST ARTIFICIAL CHROMOSOMES FROM A TOTAL HUMAN GENOME LIBRARY, NATURE GENETICS 1: 222 (1992).
3. CLERMONT, O, USE OF GENETIC AND PHYSICAL MAPPING TO LOCATE THE SPINAL MUSCULAR-ATROPHY LOCUS BETWEEN 2 NEW HIGHLY POLYMORPHIC DNA MARKERS, AMERICAN JOURNAL OF HUMAN GENETICS 54: 687 (1994).
4. CZEIZEL, A, A HUNGARIAN STUDY ON WERDNIG-HOFFMANN DISEASE, JOURNAL OF MEDICAL GENETICS 26: 761 (1989).
5. DANIELS, R.J., LINKAGE ANALYSIS OF SPINAL MUSCULAR-ATROPHY, GENOMICS 12: 335 (1992).
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