Gaspar, HaraldUniversität HeidelbergHeidelberg
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- Moog, Ute (1)
- Sutter, Christian (1)
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- Kisselbach, Jana (1)
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Publications in heiBIB 
- Callewaert, Bert: Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa / Bert Callewaert, Chi-Ting Su, Tim Van Damme, Philip Vlummens, Fransiska Malfait, Olivier Vanakker, B… , 2013. - 11 S.
In: Human mutation, ISSN 1098-1004. 34(2013), 1, Seite 111-121
DOI: 10.1002/humu.22165
- Webb, Bryn D.: HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1−/−mice / Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian R. Schubert, Ke Hao, Caroline … , July 5, 2012. - 9 S.
In: The American journal of human genetics, ISSN 1537-6605. 91(2012), 1, Seite 171-179
DOI: 10.1016/j.ajhg.2012.05.018
- Evers, Christina: Hepatoblastoma in two siblings and familial adenomatous polyposis : causal nexus or coincidence? / Christina Evers, Harald Gaspar, Matthias Kloor, Gergana Bozukova, Martina Kadmon, Monika Keller, Chr… , September 2012. - 5 S.
In: Familial cancer, ISSN 1573-7292. 11(2012), 3, Seite 529-533
DOI: 10.1007/s10689-012-9538-2
- Huth, Cathrin: The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors / Cathrin Huth, Matthias Kloor, Anita Y. Voigt, Gergana Bozukova, Christina Evers, Harald Gaspar, Mirj… . - 6 S.
In: Modern pathology, ISSN 1530-0285. 25(2012), 6, S. 911-916
DOI: 10.1038/modpathol.2012.30
- Solomon, Benjamin: Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog / Benjamin D. Solomon, Kelly A. Bear, Adrian Wyllie, Amelia A. Keaton, Christele Dubourg, Veronique Da… . - 7 S.
In: Journal of medical genetics, ISSN 1468-6244. 49(2012), 7, S. 473-479
DOI: 10.1136/jmedgenet-2012-101008
- Gribouval, Olivier: Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis / Olivier Gribouval, Vincent Morinière, Audrey Pawtowski, Christelle Arrondel, Satu-Leena Sallinen, Ca… . - 11 S.
In: Human mutation, ISSN 1098-1004. 33(2012), 2, S. 316-326
DOI: 10.1002/humu.21661
- Aidery, Parwez: Identification and functional characterization of the novel human ether-a-go-go-related gene (hERG) R744P mutant associated with hereditary long QT syndrome 2 / Parwez Aidery, Jana Kisselbach, Harald Gaspar, Ioana Baldea, Patrick A. Schweizer, Rüdiger Becker, H… , 30 January 2012. - 6 S.
In: Biochemical and biophysical research communications, ISSN 0006-291X. 418(2012), 4, Seite 830-835
DOI: 10.1016/j.bbrc.2012.01.118
- Gaspar, Harald: Ätiologie und genetische Aspekte der Möbius-Sequenz / H. Gaspar, 20. Juni 2010. - 4 S.
In: Der Ophthalmologe, ISSN 1433-0423. 107(2010), 8, Seite 704-707
DOI: 10.1007/s00347-010-2146-3
