Somatic mutations are not observed by exome sequencing of lymphocyte DNA from monozygotic twins discordant for congenital hypothyroidism due to thyroid dysgenesis

Hormone Research in Paediatrics

Volumn 83, Issue 2, 2015, Pages 79-85

  Magne, Fabien ^a,b   Serpa, Roman ^b   Van Vliet, Guy ^a   Samuels, Mark E ^a,b   Deladoëy, Johnny ^a,b  

^a UNIVERSITY OF MONTREAL   (Canada)

^b UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

Congenital hypothyroidism; Exome sequencing; Monozygotic twins

Indexed keywords

DNA;

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HYPOTHYROIDISM; ECTOPIC THYROID GLAND; EXOME; FEMALE; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME; HUMAN; INFANT; LYMPHOCYTE; MALE; MONOZYGOTIC TWINS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SOMATIC MUTATION; THYROID DYSGENESIS; CLINICAL TRIAL; GENETICS; HIGH THROUGHPUT SEQUENCING; MUTATION; TWINS;

CONGENITAL HYPOTHYROIDISM; DNA; EXOME; FEMALE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; MUTATION; THYROID DYSGENESIS; TWINS, MONOZYGOTIC;

EID: 84925359436     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000365393     Document Type: Article

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