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1 Ergebnisse
1
Whole-Exome Sequencing Identifies Mutated C12orf57 in Reces..:
Akizu, Naiara
;
Shembesh, Nuri M
;
Ben-Omran, Tawfeg
...
qt02z0s86m. , 2013
Link:
https://escholarship.org/uc/item/02z0s86m
RT Journal T1
Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt02z0s86m&Exemplar=1&LAN=DE A1 Akizu, Naiara A1 Shembesh, Nuri M A1 Ben-Omran, Tawfeg A1 Bastaki, Laila A1 Al-Tawari, Asma A1 Zaki, Maha S A1 Koul, Roshan A1 Spencer, Emily A1 Rosti, Rasim Ozgur A1 Scott, Eric A1 Nickerson, Elizabeth A1 Gabriel, Stacey A1 da Gente, Gilberto A1 Li, Jiang A1 Deardorff, Matthew A A1 Conlin, Laura K A1 Horton, Margaret A A1 Zackai, Elaine H A1 Sherr, Elliott H A1 Gleeson, Joseph G PB eScholarship, University of California YR 2013 K1 Biological Sciences K1 Genetics K1 Pediatric K1 Clinical Research K1 Agenesis of Corpus Callosum K1 Amino Acid Sequence K1 Cerebral Cortex K1 Codon K1 Corpus Callosum K1 Exome K1 Female K1 Genetic Predisposition to Disease K1 Humans K1 Male K1 Methionine K1 Molecular Sequence Data K1 Mutation K1 Sequence Analysis K1 DNA K1 Medical and Health Sciences K1 Genetics & Heredity K1 Biomedical and clinical sciences K1 Health sciences JF qt02z0s86m LK http://dx.doi.org/https://escholarship.org/uc/item/02z0s86m DO https://escholarship.org/uc/item/02z0s86m SF ELIB - SuUB Bremen
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