Characteristics of dystrophin gene mutations among Chinese patients as revealed by multiplex ligation-dependent probe amplification.

Genetic testing and molecular biomarkers

Volumn 13, Issue 1, 2009, Pages 23-30

  Wang, Qian ^a   Li Ling, Jesse ^a   Lin, Changkun ^a   Wu, Yingyu ^a   Sun, Kailai ^a   Ma, Hongwei ^a   Jin, Chunlian ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; MICROSATELLITE DNA; PRIMER DNA;

ARTICLE; ASIAN; CHINA; COMPARATIVE STUDY; DUCHENNE MUSCULAR DYSTROPHY; EVALUATION; EXON; FEMALE; GENETIC LINKAGE; GENETIC SCREENING; GENETICS; HUMAN; MALE; METHODOLOGY; MOLECULAR GENETICS; MUTATION; NEWBORN; NUCLEIC ACID AMPLIFICATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS;

ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHINA; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DYSTROPHIN; EXONS; FEMALE; GENETIC SCREENING; HUMANS; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHY, DUCHENNE; MUTATION; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 67049165581     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2008.0059     Document Type: Article

References (0)