1
0
0
(1 - 48 von 69
)
CFnewslet.68Cystic Fibrosis Mutation Database
www.genet.sickkids.on.ca
Sabina Liechti-Gallati 1716+2T->C T->C at 1716+2 intron splice mutation Institut de Claustres M, 10 Biologie Guittard C, Montpellier, Carles S (Feb 2) ...
November FDP.Die Liberalen
www.fdp.ch
— PD Sabina Liechti-Gallati, Bern. Forum 3: Gentechnik in der Medizin. (Pharmaprodukte; Organspende; transgene Tiere). Prof. Dr. Felix Gutzwiller.
CFnewslet.68
www.genet.sickkids.on.ca
Contact: Dr. Sabina Liechti-Gallati 1716+2T->C T->C at 1716+2 intron splice mutation Institut de Claustres M
The Lancet, 16 August 1986, Volume 328, Issue 8503The Lancet
www.thelancet.com
Sabina Liechti-Gallati,; Suzanne Braga,; Hans Moser,; Hans Hirsiger. View at ScienceDirect. p393. p393. DNA TYPING TO AVOID NEED FOR PRENATAL DIAGNOSIS OF ...
shows tRNASer(UCN) mutations in a subgroup withJournal of Medical Genetics
jmg.bmj.com
von M Jaksch · · Zitiert von: 94 — Michaela Jaksch, Sabine Hofmann, Stephanie Kleinle, Sabina Liechti-Gallati,. Dieter E Pongratz, Josef Miuller-Hocker, Kerry B Jedele, Thomas Meitinger,. Klaus ...
Journal of Allergy and Clinical Immunology - Vol n° 1 - EM...
www.em-consulte.com
Marianne Rohrbach, Urs Frey, Richard Kraemer, Sabina Liechti-Gallati. fleche ouvert Plan fleche ouvert Plan Ajouter à ma bibliothèque Retirer bibliothèque.
Frequency of mitochondrial transfer RNA mutations and deletions in...
jmg.bmj.com
Sabina Liechti-Gallati b, Hanns Lochmuller e, Rita Horvath a; a Metabolic Disease Centre Munich-Schwabing
Dr. Ronald G. Crystal, MD | New York, NY | PulmonologistUS News Health
health.usnews.com
Rudeberg, C W Sommer, Sabina Liechti-Gallati, Richard Kraemer, R C Hubbard, Ronald G. Crystal. Direct in vivo adenovirus-mediated gene transfer to salivary ...
Dr. Charles T. Caskey, MD | Houston, TX - US News Healthhealth.usnews.com › Doctors
health.usnews.com
... H. Gilgenkrantz, Jean-Claude Kaplan, F.H. Herrmann, Claudine Junien, Catherine Boileau, Sabina Liechti-Gallati, M. Lindlöf, T. Matsumoto, Norio Niikawa, ...
PreisverleihungenPädiatrie Schweiz
www.paediatrieschweiz.ch
1999 Sabina Liechti-Gallati, Bern; U. Zumsteg, Basel; Claire-Anne Siegrist, Genève; Daniel Desgrandchamps, Baar; Ulrich Heininger, Basel; Bernard ...
Ornithine transcarbamylase deficiency: Characterization of gene...
journals.scholarsportal.info
Elisabeth Oppliger Leibundgut · Bendicht Wermuth · Jean‐Pierre Colombo · Sabina Liechti-Gallati ...
Burgdorfer JahrbuchUniversitätsbibliothek Bern UB
biblio.unibe.ch
Die in Burgdorf aufgewachsene Sabina Liechti-Gallati erhält anlässlich des Kongresses der Pädiatrischen Forschung der. Schweiz in Bern den Nestle-Preis für ...
Clonal Analysis of Human Tumors with M27,6, a Highly ...Europe PMC
europepmc.org
von MF Fey · · Zitiert von: 116 — Hinds,11 Arthur Zimmermann," Sabina Liechti-Gallati,** Hans Gerber,'. Hugo Studer,§ and Andreas Tobler". *Institute ofMedical Oncology, Inselspital, Berne ...
Confirmation of Prenatal Diagnosis Results of X-Linked ...ProQuest
search.proquest.com
von SM Tanner · · Zitiert von: 42 — ... Sabina Liechti-Gallati. 1Department of Clinical Research, Human Molecular Genetics, Insel spital/Kinderklinik G2/811, University of Berne, Berne,. Switzerland.
Mitochondriopathien in der KardiologieZeitschrift Medizinische Genetik
www.medgenetik.de
Sabina Liechti-Gallati. Molekulare Humangenetik. Medizinische Universitätskinderklinik. Universität Bern, Inselspital. CH Bern. Tel + ... sabina.liechti@ ...
Mutations in the MTM1 Gene Implicated in X-Linked ...Oxford Academic
academic.oup.com
von J Laporte · · Zitiert von: 148 — Sabina Liechti-Gallati ,. Sabina Liechti-Gallati. 2. Department of Clinical Research, University of Berne. , Berne, Switzerland. Search for other works by ...
A 900-kb Cosmid Contig and 10 New Transcripts within the ...ScienceDirect.com
www.sciencedirect.com
von P Kioschis · · Zitiert von: 25 — , Johannes F. Coy a , Jocelyn Laporte b , Sabina Liechti-Gallati c , Annemarie Poustka a. Show more. Add to Mendeley. Share. Cite. https://doi.org
Confirmation of prenatal diagnosis results of X-linked ...Archive ouverte HAL
hal.science
von SM Tanner · · Zitiert von: 42 — ... Sabina Liechti-Gallati (1). Afficher plus de détails. 1 UNIBE - Universität Bern / University of Bern 2 IGBMC - Institut de Génétique et de Biologie ...
An explanation for the phenotypic differences between ...ScienceDirect.com
www.sciencedirect.com
von AP Monaco · · Zitiert von: — ... overlay panel. Anthony P. Monaco ∗ † a , Corlee J. Bertelson ∗ a , Sabina Liechti-Gallati ‡ b , Hans Moser ‡ b , Louis M. Kunkel ∗ † § a. Show more. Add to ...
Genomic organization of the MTM1 gene implicated in X- ...Archive ouverte HAL
hal.science
von J Laporte · · Zitiert von: 28 — ... Sabina Liechti-Gallati , Jean-Louis Mandel (1, 2). Afficher plus de détails. 1 IGBMC - Institut de génétique et biologie moléculaire et ...
Die Dozenten der Berner Hochschule von 1980YUMPU
www.yumpu.com
— Sabina Liechti-Gallati, für medizinische Molekulargenetik; Dr. Christoph. Meier, für propädeutische Mathematik; PD Dr. Andreas Werner ...
Parental origin and germline mosaicism of deletions ...Springer
link.springer.com
von AJ van Essen · · Zitiert von: 128 — Sabina Liechti-Gallati. Instituto di Clinico e Biologica Dell'Eta' Evolutiva, Università Studi Cagliari, Via Jenner s/n, I , Cagliari, Italy. Marie A ...
(PDF) Genotype/Phenotype Association in Cystic Fibrosis:Amanote Research
research.amanote.com
Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations by Sabina Liechti-Gallati, Irene Bonsall,
Association Between Haplotypes and Specific Mutations ...Amanote Research
research.amanote.com
Association Between Haplotypes and Specific Mutations in Swiss Cystic Fibrosis Families by Sabina Liechti-Gallati, Naseem Malik, Mualla Alkan, Marco.
161 Severe clinical course in cystic fibrosis (CF) patient ...Nature
www.nature.com
von S Liechti-Gallati · — Sabina Liechti-Gallati & ... Authors and Affiliations. Department of Pediatrics, University of Berne,. Sabina Liechti-Gallati & Richard Kramer.
Gentechkritisches Forum GenAu, BernLycos.com
forumgenau.tripod.com
Humangenetik mit (Dr. Sabina Liechti-Gallati); Juni 1996: Forum 3: Technologiefolgenabschätzung, politische Partizipation (Dr. Michael Altmann). -> Hauptseite.
Two buffer PAGE system-based SSCP/HD analysisNature
www.nature.com
von S Liechti-Gallati · · Zitiert von: 132 — Dr Sabina Liechti-Gallati, PhD,. Molecular Human Genetics, Children's Hospital/Inselspital,. CH Bern/Switzerland. Tel: + ; Fax: + Seiten
www.nature.com › pediatric research › articlesNucleotidase Activities in Cultured Skin Fibroblasts from Patients ...
www.nature.com
von S Liechti-Gallati · · Zitiert von: 21 — Abnormal Growth Kinetics and 5′-Nucleotidase Activities in Cultured Skin Fibroblasts from Patients with Duchenne Muscular Dystrophy. Sabina Liechti-Gallati ...
11،13،20و21 و ژن CFTR بوسيله روشهاي ARMS-PCR، SSCP ...SID
www.sid.ir
von M Amiri — Sabina Liechti-Gallati, vreni schneider and et al (1999). European Journal of Human Genetics. 7, T. onay, O. Topaloglu and et al (1998). Hum ...
58th ENMC Workshop: Myotubular Myopathy 20–22 March ...nmd-journal.com
www.nmd-journal.com
von C Wallgren-Pettersson · · Zitiert von: 9 — Sabina Liechti-Gallati, Berne, Switzerland. Dr. Bernard van Oost, Utrecht, The Netherlands. Dr. Karen Helene Orstavik, Oslo, Norway. Dr. Caroline Sewry, London ...
A variant in the gene for GM-CSF, I117T, is associated with ...Journal of Allergy and Clinical Immunology
www.jacionline.org
von M Rohrbach · · Zitiert von: 30 — Sabina Liechti-Gallati, PhD. Sabina Liechti-Gallati. Affiliations. Human Molecular Genetics, the Department of Clinical Research Berne, Switzerland. Search for ...
Analysis of amplified DNA from exon 5 in the family ...ResearchGate
www.researchgate.net
Sabina Liechti-Gallati · Jean-Pierre Colombo · Bendicht Wermuth. Ornithine transcarbamylase (OTC) deficiency, the most ...
Anthony P. Monaco: Medicine H-index & AwardsResearch.com
research.com
Bertelson;Sabina Liechti-Gallati;Hans Moser. Genomics (1988) Citations. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy ...
Chronic Metabolic Alkalosis: Not Uncommon in Young ...Karger Publishers
karger.com
von G Pedroli · · Zitiert von: 26 — Sabina Liechti-Gallati;. Sabina Liechti-Gallati. Department of Pediatrics, University of Bern, Switzerland. Search for other works by this ...
Deletions in Xq28 in two boys with myotubular myopathy ...Semantic Scholar
www.semanticscholar.org
... : Mapping the gene to Xq28 · Sabina Liechti-GallatiB. Muller +5 authors. S. Braga. Medicine. Neuromuscular Disorders Citations. Add to Library.
Duchenne muscular dystrophy quantification of ...AI Chat for scientific PDFs | SciSpace
typeset.io
Bertelson,Sabina Liechti-Gallati,H. Moser,Louis M. Kunkel +5 moreBoston Children's Hospital,Harvard University Dec Genomics. Show Less. TL;DR: A ...
Genomic organization of the MTM1 gene implicated in X- ...Archive ouverte HAL
hal.archives-ouvertes.fr
... Sabina Liechti-Gallati , Jean-Louis Mandel (1, 2). Afficher plus de détails. 1 IGBMC - Institut de génétique et biologie moléculaire et cellulaire 2 IGBMC ...
Histopathological Alterations in Muscle Tissue and their ...Hilaris Publishing SRL
www.hilarispublisher.com
Monaco, Anthony P., Corlee J. Bertelson, Sabina Liechti-Gallati and Hans Moser, et al. "An explanation for the phenotypic differences between patients ...
Jocelyn LAPORTEIGBMC
www.igbmc.fr
Sabina Liechti-Gallati. Human Mutation ; Volume: 11 ; Page: HAL DOI Characterization of mutations in the myotubularin gene in twenty six patients ...
July 1999Journal of Allergy and Clinical Immunology
www.jacionline.org
Sabina Liechti-Gallati. Published in issue: July p Full-Text HTML · PDF. Editorial Board. Editorial Board. Published in issue: July p20A.
Muscle Histopathological Changes and Consequences in ...Hilaris Publishing SRL
www.hilarispublisher.com
Bertelson, Sabina Liechti-Gallati, and Hans Moser, et al. "An explanation for the phenotypic differences between patients bearing partial deletions of the ...
Regulation of MTMR2 by Phosphorylation - bac-lac.gc.cabac-lac.gc.ca
central.bac-lac.gc.ca
von N Franklin · — Blondeau, Sabina Liechti-Gallati, and Jean-Louis Mandel. MTM1 Mutations in X-Linked. Myotubular Myopathy. Human Mutation. 15: (2000).
Regulation of MTMR2 by Phosphorylation: Subcellular ...University of Windsor
scholar.uwindsor.ca
von N Franklin · — Blondeau, Sabina Liechti-Gallati, and Jean-Louis Mandel. MTM1 Mutations in X-Linked. Myotubular Myopathy. Human Mutation. 15: (2000).
Volume 36 Issue 1-2 | Hormone Research in PaediatricsKarger Publishers
karger.com
Mullis; Sabina Liechti-Gallati; Lucia Di Silvio; Charles G.D. Brook; Auristela F. Paes-Alves. Hormone Research (1991) 36 (1-2): 4–8. https://doi.org
[PDF] Mutations in the MTM1 gene implicated in X-linked ...Semantic Scholar
www.semanticscholar.org
+4 authors. Sabina Liechti-Gallati. Medicine. Neuromuscular Disorders Citations. Add to Library. Alert. A novel mutation in exon b (R259C) of the ...
antiporter mRNA in biliary epithelial cells and in hepatocytesJournal of Hepatology
www.journal-of-hepatology.eu
von U Marti · · Zitiert von: 22 — Sabina Liechti-Gallati. Sabina Liechti-Gallati. Affiliations. Department of Clinical Pharmacology, University of Berne, Berne, Switzerland. Search for articles ...
single eltern Bellinzona Schweiz : heute single party in ...Wir für Möckmühl
yiliqakuk.summerofpainting.de
Belli, Genf Sabina Liechti-Gallati, Bern U. Gallen; Nathalie Farpour, Genf Paul Imbach, Uettligen Eugen Boltshauser, Zürich Sepp Holtz, Zürich Walter Bär ...
Нарушения системы гемостаза при инфекционном ...disserCat
www.dissercat.com
... Sabina Liechti-Gallati, Beat J. Meyer // The Lancet V №№ Murdoch, D.R. Clinical presentation, etiology, and outcome of ...
Alle Infos zum Namen "Sabina Liechti"
Verwandte Suchanfragen zu Sabina Liechti
| Elisabeth Oppliger Hans Moser Martin Kistler | Anna Rüdeberg Lisa Hoyer Michael Raff | Monica Bussi-Holtmann Nadja Zürcher |
Person "Liechti" (4) Vorname "Sabina" (4594) Name "Liechti" (241) |
sortiert nach Relevanz / Datum