2005
ZORA-Hinweis zur Angaben der Autoren
- In der exportierbaren Liste werden Publikationen mit weniger als 30 Autoren 1:1 in ZORA übernommen. Es werden keine Autorennamen gelöscht. --> Grund: vollständige Metadaten pro Publikation, auch zur weiteren Verwendung (z.B. in der Swisscovery).
- Bei Publikationen mit mehr (>30) Autoren werden die Autoren beim Import automatisch auf die Zahl 30 gekürzt. Im selben Schritt wird ein "et al." erstellt. Wenn dadurch UZH-Autoren ausgelassen werden, wurden sie am Ende, nach "et al.", hinzugefügt.
- Mehr Information: Varia | Universitätsbibliothek Zürich | UZH
- Für die vollständige Auflistung der Autoren in der Reihenfolge ihrer Veröffentlichung verwenden Sie bitte die Textdatei am Ende dieser Seite.
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Publications
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Mice Null for Frizzled4 (Fzd4−/−) Are Infertile and Exhibit Impaired Corpora Lutea Formation and Function1. Biology of Reproduction, 73(6):1135-1146.
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Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram. Investigative Ophthalmology & Visual Science, 46(11):4328-4335.
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Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature. Investigative Ophthalmology & Visual Science, 46(9):3372-3382.
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Fetal loss in homozygous mutant Norrie disease mice: A new role of Norrin in reproduction. Genesis, 42(4):253-262.
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A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9. American Journal of Medical Genetics. Part A, 136A(1):31-37.
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Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. European Journal of Medical Genetics, 48(3):319-327.
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Chromosome Aberrations. In: Panteliadis, Christos P; Korinthenberg, Rudolf. Paediatric Neurology : Theory and Practice. Stuttgart, New York: Georg Thieme Verlag, 235-251.
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An unusual reciprocal translocation detected by subtelomeric FISH: interstitial and not terminal. American Journal of Medical Genetics. Part A, 135(1):86-90.
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Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21. European Journal of Medical Genetics, 48(2):167-174.
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Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome. American Journal of Medical Genetics. Part A, 134A(1):3-11.
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Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. American Journal of Human Genetics, 76(4):572-80.
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Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. Molecular Vision, 11:179-183.
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Ectopic Norrin Induces Growth of Ocular Capillaries and Restores Normal Retinal Angiogenesis in Norrie Disease Mutant Mice. Journal of Neuroscience, 25(7):1701-1710.
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Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics. Part A, 132A(1):1-7.
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M-FISH applications in clinical genetics. Genetic Counseling, 16(3):257-68.
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A case with de novo interstitial deletion of chromosome 7q21.1-q22. Genetic Counseling, 16(2):155-9.
Textdatei
So J, Suckow V, Kijas Z, Kalscheuer V, Moser B, Winter J, Baars M, Firth H, Lunt P, Hamel B, Meinecke P, Moraine C, Odent S, Schinzel A, van der Smagt JJ, Devriendt K, Albrecht B, Gillessen-Kaesbach G, van der Burgt I, Petrij F, Faivre L, McGaughranJ, McKenzie F, Opitz JM, Cox T, Schweiger S Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations Am J Med Genet 2005; 132A: 1-7
Wey E, Bartholdi D, Riegel M, Nazlican H, Horsthemke B, Schinzel A, Baumer A Mosaic Imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome Eur J Hum Genet 2005; 13:273-277
Roelfsema JH, White SJ, Ariyürek Y, Bartholdi D, Niedrist D, Papadia F, Bacino CA, den Dunnen JT, van Ommen G-JB, Breuning MH, Hennekam RC, Peters DJM Genetic heterogeneity in Rubinstein-Taybi syndrome: Mutations in both the CBP and EP300 genes cause disease Am J Hum Genet 2005;76:572-580
Schinzel A Chromosome Aberrations pp. 235-251, in: Paediatric Neurology. Theory and Practice. Ed. Christos P. Panteliadis and Rudolf Korinthenberg, 2005. Georg Thieme, Stuttgart-New York
De Scipio C, Schneider L, Young TL, Wassermann N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AGL, Guichet A, Dobyns WE, Toutain A, Spinner NB, Krantz ID Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome Am J Med Genet 2005;134A:3-11
Riegel M, Hargreaves P, Baumer A, Guc-Scekic M, Ignjatovic M, Schinzel A Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21 Eur J Med Genet 2005;48:167-174
Riegel M, Baumer A, Süss J, Schinzel A An unusual reciprocal translocation detected by subtelomeric FISH: Interstitial and not terminal Am J Med Genet 2005; 135A:86-90
Kloeckener-Gruissem B, Betts DR, Zankl A, Berger W, Güngör T A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9 Am J Med Genet 2005; 136A/138A:31-37/19
Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns J-P, Liehr T Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype Eur J Med Genet 2005; 48:319-327
Manguoglu E, Berker-Karaüzüm S, Baumer A, Mihçi E, Taçoy S, Lüleci G, Schinzel A A case with de novo interstitial deletion of chromosome 7q21.1-q22 Genet Couns 2005;16:155-159