|
Volumn 58, Issue 3, 2010, Pages 436-440
|
Clinical profile and molecular diagnosis in patients of facioscapulohumeral dystrophy from Indian subcontinent
|
Author keywords
4q35; BlnI; EcoRI; facioscapulohumeral dystrophy
|
Indexed keywords
GENOMIC DNA;
TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;
NUCLEAR PROTEIN;
ADULT;
ARTICLE;
CLINICAL ARTICLE;
CLINICAL FEATURE;
DISEASE COURSE;
DNA PROBE;
ELECTROMYOGRAPHY;
FACE MUSCLE;
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY;
FAMILY COUNSELING;
FEMALE;
GENETIC COUNSELING;
HUMAN;
HUMERUS;
INDIAN;
MALE;
MYOPATHY;
PELVIC GIRDLE;
PERONEUS MUSCLE;
RETROSPECTIVE STUDY;
SCAPULA;
SOUTHERN BLOTTING;
ADOLESCENT;
CLASSIFICATION;
EPIDEMIOLOGY;
FAMILY HEALTH;
GENETICS;
INDIA;
MIDDLE AGED;
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL;
NUCLEOTIDE SEQUENCE;
PROCEDURES;
RESTRICTION MAPPING;
YOUNG ADULT;
ADOLESCENT;
ADULT;
DISEASE PROGRESSION;
DNA MUTATIONAL ANALYSIS;
ELECTROMYOGRAPHY;
FAMILY HEALTH;
FEMALE;
HUMANS;
INDIA;
MALE;
MIDDLE AGED;
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL;
NUCLEAR PROTEINS;
RESTRICTION MAPPING;
YOUNG ADULT;
|
EID: 77955070658
PISSN: 00283886
EISSN: 19984022
Source Type: Journal
DOI: 10.4103/0028-3886.66456 Document Type: Article |
Times cited : (3)
|
References (12)
|