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1 Ergebnisse
1
Submicroscopic Deletions at 13q32.1 Cause Congenital Microc..:
Fares-Taie, Lucas
;
Gerber, Sylvie
;
Tawara, Akihiko
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2015.01.014. , 2015
Link:
https://univ-rennes.hal.science/hal-01134461
RT Journal T1
Submicroscopic Deletions at 13q32.1 Cause Congenital Microcoria
UL https://suche.suub.uni-bremen.de/peid=base-ftunivrennes1hal:oai:HAL:hal-01134461v1&Exemplar=1&LAN=DE A1 Fares-Taie, Lucas A1 Gerber, Sylvie A1 Tawara, Akihiko A1 Ramirez-Miranda, Arturo A1 Douet, Jean-Yves A1 Verdin, Hannah A1 Guilloux, Antoine A1 Zenteno, Juan C A1 Kondo, Hiroyuki A1 Moisset, Hugo A1 Passet, Bruno A1 Yamamoto, Ken A1 Iwai, Masaru A1 Tanaka, Toshihiro A1 Nakamura, Yusuke A1 Kimura, Wataru A1 Bole-Feysot, Christine A1 Vilotte, Marthe A1 Odent, Sylvie A1 Vilotte, Jean-Luc A1 Munnich, Arnold A1 Regnier, Alain A1 Chassaing, Nicolas A1 de Baere, Elfride A1 Raymond-Letron, Isabelle A1 Kaplan, Josseline A1 Calvas, Patrick A1 Roche, Olivier A1 Rozet, Jean-Michel PB HAL CCSD; Elsevier (Cell Press) YR 2015 K1 MESH: Base Sequence K1 Chromosome Deletion* K1 Chromosomes K1 Human K1 Pair 13/genetics* K1 Comparative Genomic Hybridization K1 Gene Components K1 Genes K1 Dominant/genetics K1 Humans K1 Hydro-Lyases/genetics K1 Molecular Sequence Data K1 Mutation/genetics K1 Oligonucleotide Array Sequence Analysis K1 Pedigree K1 Pupil Disorders/congenital* K1 Pupil Disorders/genetics K1 Pupil Disorders/pathology K1 Receptors K1 Cell Surface/genetics* K1 Sequence Analysis K1 DNA K1 [SDV]Life Sciences [q-bio] JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2015.01.014 LK http://dx.doi.org/https://univ-rennes.hal.science/hal-01134461 DO https://univ-rennes.hal.science/hal-01134461 SF ELIB - SuUB Bremen
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