Erratum: Is the novel SCKL3 at 14q23 the predominant Seckel locus?(European Journal of Human Genetics (2003) 11 (851-857) DOI: 10.1038/sj.ejhg.5201057);Is the novel SCKL3 at 14q23 the predominant Seckel locus?

European Journal of Human Genetics

Volumn 11, Issue 11, 2003, Pages 851-857

  Kilinç, Mehmet Okyay ^a,e   Ninis, Vasiliki Ninidu ^a   Uǧur, Sibel Aylin ^a   Tüysüz, Beyhan ^b   Seven, Mehmet ^b   Balci, Sevim ^c   Goodship, Judith ^d   Tolun, Aslihan ^a  

^a BOGAZICI UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

^c HACETTEPE UNIVERSITY   (Turkey)

^d NEWCASTLE UNIVERSITY   (United Kingdom)

^e University of Louisville School of Medicine   (United States)

Author keywords

SCKL; SCKL3; Seckel syndrome; Turkish

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 18P; CHROMOSOME 3Q; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; DNA REPAIR; FAMILY; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; INFANT; MALE; PHENOTYPE; PRIORITY JOURNAL; SECKEL SYNDROME; SIBLING; TURKEY (REPUBLIC);

EID: 0242441476     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.258     Document Type: Erratum

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