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Резултати

Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer   [2004]

McKay, JD; Thompson, D; Lesueur, F; Stankov, Karmen  ; Pastore, A; Watfah, C; Strolz, S; Riccabona, G; Moncayo, R; Romeo, G;
Goldgar, DE;

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy   [2010]

Otto, E. A.; Ramaswami, G.; Janssen, S.; Chaki, M.; Allen, S. J.; Zhou, W.; Airik, R.; Hurd, T. W.; Ghosh, A. K.; Wolf, M. T.;
Hoppe, B.; Neuhaus, T. J.; Bockenhauer, D.; Milford, D. V.; Soliman, N. A.; Antignac, C.; Saunier, S.; Johnson, C. A.; Hildebrandt, F.;

Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia   [2010]

Stanke, F.; Becker, T.; Kumar, V.; Hedtfeld, S.; Becker, C.; Cuppens, H.; Tamm, S.; Yarden, J.; Laabs, U.; Siebert, B.;
Fernandez, L.; Macek, M.; Radojković, Dragica  ; Ballmann, M.; Greipel, J.; Cassiman, J.-J.; Wienker, T. F.; Tummler, B.;

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype   [2004]

Yarden, J; Radojkovic, Dragica P; De, Boeck K; Macek, M; Zemkova, D; Vavrova, V; Vlietinck, R; Cassiman, JJ; Cuppens, H

Poland syndrome associated with morning glory syndrome (coloboma of the optic disk)   [1986]

Vranešević, Dušan; Pišteljić, DT; Apostolski, Slobodan

Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders   [2021]

Nicita, Francesco; ...; Brankovic, Vesna; ...; (broj, koautora 25)

Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study   [2021]

Nuovo, Sara; ...; Brankovic, Vesna; ...; (broj, koautora 35)

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