Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays

Human Mutation

Volumn 28, Issue 3, 2007, Pages 235-242

  Stanczak, Christopher M ^a   Chen, Zugen ^a   Zhang, Yao Hua ^a   Nelson, Stanley F ^a   McCabe, Edward R B ^a,b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c MATTEL CHILDREN S HOSPITAL   (United States)

Author keywords

Contiguous gene syndrome; Deletion mapping array; Glycerol kinase deficiency; Molecular cytogenetics; SNP mapping array

Indexed keywords

CELL NUCLEUS RECEPTOR; GENOMIC DNA; GLYCEROL; GLYCEROL KINASE;

ADRENAL DISEASE; ARTICLE; CHROMOSOME XP; CONTROLLED STUDY; CYTOGENETICS; DNA MICROARRAY; DUCHENNE MUSCULAR DYSTROPHY; ENZYME DEFICIENCY; FEMALE; GENE DELETION; GENE MAPPING; GENOTYPE; HUMAN; HUMAN CELL; HYPOPLASIA; LIVE BIRTH; LYMPHOBLASTOID CELL LINE; MALE; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES;

CELLS, CULTURED; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, X; FEMALE; GENE DOSAGE; GENETIC SCREENING; GLYCEROL KINASE; HUMANS; MALE; MICROARRAY ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; RANDOM ALLOCATION; SYNDROME;

EID: 33847226937     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20424     Document Type: Article

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