LOT1 (ZAC1/PLAGL1) as member of an imprinted gene network does not harbor Silver-Russell specific variants

Journal of Pediatric Endocrinology and Metabolism

Volumn 22, Issue 6, 2009, Pages 555-559

  Jäger, Susanne ^a   Schönherr, Nadine ^a   Spengler, Sabrina ^a   Ranke, Michael B ^b   Wollmann, Hartmut A ^b   Binder, Gerhard ^b   Eggermann, Thomas ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b Institute of Molecular Cell Biology   (Germany)

Author keywords

Chromosome 6q24 25; LOT1; PLAGL1; Polymorphisms; Silver Russell syndrome; ZAC1

Indexed keywords

GENOMIC DNA;

ARTICLE; CHROMOSOME 6Q; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; GENE; GENE MUTATION; GROWTH RETARDATION; HUMAN; HUMAN CELL; INTRAUTERINE GROWTH RETARDATION; LOT1 GENE; NUCLEOTIDE SEQUENCE; PLAGL1 GENE; POSTNATAL GROWTH RETARDATION; REAL TIME POLYMERASE CHAIN REACTION; SCREENING; SILVER RUSSELL SYNDROME; SINGLE STRAND CONFORMATION POLYMORPHISM; ZAC1 GENE;

EID: 67651036882     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2009.22.6.555     Document Type: Article

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