No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders

American Journal of Medical Genetics, Part A

Volumn 170, Issue 1, 2016, Pages 283-284

  Müller, Anne ^a   Soellner, Lukas ^a   Binder, Gerhard ^b   Begemann, Matthias ^a   Eggermann, Thomas ^a  

^a UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^b UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

Beckwith Wiedemann syndrome; IGF2 mutations; Silver Russell syndrome

Indexed keywords

SOMATOMEDIN; SOMATOMEDIN RECEPTOR; IGF2 PROTEIN, HUMAN; SOMATOMEDIN B;

ALLELE; CELL PROLIFERATION; COPY NUMBER VARIATION; DISEASE ASSOCIATION; GENE; GENE MUTATION; GENETIC VARIABILITY; GENOME IMPRINTING; GROWTH RETARDATION; HUMAN; IGF2 GENE; LETTER; MAJOR CLINICAL STUDY; MOUSE; NONHUMAN; PERINATAL PERIOD; PHENOTYPE; POSTNATAL GROWTH; PRENATAL PERIOD; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11; GENETIC SCREENING; GENETICS; INTRAUTERINE GROWTH RETARDATION;

BECKWITH-WIEDEMANN SYNDROME; CHROMOSOMES, HUMAN, PAIR 11; FETAL GROWTH RETARDATION; GENETIC TESTING; GENOMIC IMPRINTING; HUMANS; INSULIN-LIKE GROWTH FACTOR II;

EID: 84955716389     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.37416     Document Type: Letter

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