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Clinical and molecular delineation of the 17q microdeletion ...jmg.bmj.com › › jmg info
jmg.bmj.com
... Janine Wagenstaller PubMed articlesGoogle scholar articles; Ana C Krepischi-Santos PubMed articlesGoogle scholar articles; Angela M Vianna-Morgante ...
Ausbildung
Identification and characterization of disease Dipòsit Digital de la UB
diposit.ub.edu
Microdeletion Syndrome 16p11.2-p12.2: Clinical and Molecular Characterization. Maja Hempel,. 1,2. * Nuria Rivera Brugués,. 1,2. Janine Wagenstaller,. 1,2.
Bücher
KARLA - Katalogportal der UB Kassel: Artikel & mehr -...
hds.hebis.de
von Janine Wagenstaller ; Stephanie Spranger ; Bettina Lorenz-Depiereux ; et al. American Journal of Human Genetics. Oct2007, Vol.
Cell signaling research papers - November - Signaling Update -...
www.signaling-gateway.org
A selection of current cell signaling primary research papers and reviews ordered by publication date.
Genetics: A Conceptual Approachbooks.google.com › books
books.google.com
For example, Janine Wagenstaller and her colleagues studied copy-number variation in 67 children with unexplained mental retardation and found that 11 (16%) ...
Dokumente zum Namen
Wagenstaller, Janine [WorldCat Identities]
www.worldcat.org
Kopplungsanalysen und Bestimmung von Kopienzahlvariationen mit Oligonukleotid-Mikroarrays by Janine Wagenstaller( Book ) 3 editions published in in ...
Delineation of a 2q Deletion in a Girl With Dysmorphic Features and ...onlinelibrary.wiley.com › doi › pdf › ajmg.a
onlinelibrary.wiley.com
Sabine Langer,1,2 Jochen B. Geigl,1,2 Janine Wagenstaller,1,2 Gaby Lederer,1,2 Maja Hempel,3. Cornelia Daumer-Haas,3 Hans-Jürgen Leifheit,4 and Michael R.
Chapter 9 Genetics | PDF | Gene Duplication | Zygosity - Scribdwww.scribd.com › document › Chapter-9-Genetics
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Janine Wagenstaller and her colleagues studied copy-number The gain of a chromosome means that there are three variation in 67 children with unexplained ...
Mutations in the lipoma HMGIC fusion partnerâ•'like 5 (LHFPL5 ...onlinelibrary.wiley.com › doi › pdf › humu
onlinelibrary.wiley.com
Edyta Rohmann,4,5 Janine Wagenstaller,9 Lies H. Hoefsloot,1 Tim M. Strom,9,10 Gudrun Nürnberg,11,12. Nermin Baserer,8 Anneke I. den Hollander,1,13 Frans ...
Wissenschaftliche Veröffentlichungen
Identification of FOXP1 deletions in three unrelated patients with...
www.ikmb.uni-kiel.de
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, Ute Moog, Bettina Lorenz-Depiereux, Sebastian Eck, Maja Hempel, Janine Wagenstaller, Alex Gawthrope, …
Veröffentlichungen allgemein
[PDF] Polymorphism Oligonucleotide Arrays in Patients with Mental Retacore.ac.uk › download › pdf
core.ac.uk
· Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz-Depiereux, Bernd Kazmierczak,. Michaela Nathrath, Dagmar Wahl, Babett Heye, ...
Publications Authored by Janine Wagenstaller | PubFacts
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Publications Authored by Janine Wagenstaller
[PDF] ÜBERBLICK - Markt Glonnmarktgemeinde-glonn.de › uploads › › gms
marktgemeinde-glonn.de
Christine Scholz, Herrmannsdorf 12. Robert Lessl, Schlacht 42. Monika Goppel, Schlacht 42. Frank Graf, Kastenseeon 11. Janine Wagenstaller, Kastenseeon 11.
Janine Wagenstaller - Deutsche Digitale Bibliothekwww.deutsche-digitale-bibliothek.de › person › gnd
www.deutsche-digitale-bibliothek.de
Janine Wagenstaller. Biologin. Geboren: 1977, Ebersberg. Hat mitgewirkt an: ... Suche: „Janine Wagenstaller“ in der DDB. Externe Links:.
Artikel & Meinungen
Wikipedia: Mikrodeletionssyndrom 2q Wikipediade.wikipedia.org › wiki
... 2q23.1; Pseudo-Angelman-Syndrom. Die Erstbeschreibung stammt aus dem Jahre durch die Humangenetikerin Janine Wagenstaller und Mitarbeiter.
DMP1 mutations in autosomal recessive hypophosphatemia implicate a...
www.nature.com
Brief Communication
Sonstiges
Copy-Number Variations Measured by Single SlidePlayerslideplayer.com › slide
slideplayer.com
1 Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation Janine Wagenstaller, ...
Fw: [AJHG-TOC] AJHG February (vol 78 no 2) Contents - Yahoo ...
groups.yahoo.com
Bettina Lorenz-Depiereux, Anna Benet-Pages, Gertrud Eckstein, Yardena Tenenbaum-Rakover, Janine Wagenstaller, Dov Tiosano, Ruth Gershoni-Baruch, ...
Janine Wagenstaller's research works | Helmholtz-Zentrum für ...www.researchgate.net › scientific-contributions › Ja...
www.researchgate.net
Janine Wagenstaller's 15 research works with citations and reads, including: Identification of FOXP1 Deletions in Three Unrelated Patients with ...
Mikrodeletionssyndrom 2q Wikiwandwww.wikiwand.com › ...
www.wikiwand.com
... 2q23.1; Pseudo-Angelman-Syndrom. Die Erstbeschreibung stammt aus dem Jahre durch die Humangenetikerin Janine Wagenstaller und Mitarbeiter.
Elisabeth Graf Riemann - Deutsch-Englisch Übersetzung | PONS
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Übersetzung Deutsch-Englisch für Elisabeth Graf Riemann im PONS Online-Wörterbuch nachschlagen! Gratis Vokabeltrainer, Verbtabellen, Aussprachefunktion.
Elisabeth Graf Riemann - nemščina-angleščina prevod | PONS
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Tu si lahko ogledate prevod nemščina-angleščina za Elisabeth Graf Riemann v PONS spletnem slovarju! Brezplačna jezikovna vadnica, tabele sklanjatev, funkcija...
Elisabeth Graf Riemann - tłumaczenie niemiecki-angielski | PONS
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Sprawdź tutaj tłumaczenei niemiecki-angielski słowa Elisabeth Graf Riemann w słowniku online PONS! Gratis trener słownictwa, tabele odmian czasowników, wymowa.
Elisabeth Graf Riemann - Translation from German into English ...en.pons.com › PONS Dictionary › German » English
en.pons.com
Anna Benet-Pages, Janine Wagenstaller PhD / MD students : Sebastian Eck , Elisabeth Graf , Thomas Wieland 2. Neurogenetics ( Guest Group – in collaboration ...
Elisabeth Graf Riemann - Translation from German into English | PONS
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Look up the German to English translation of Elisabeth Graf Riemann in the PONS online dictionary. Includes free vocabulary trainer, verb tables and...
thomas sebastian byrne - Englisch-Deutsch Übersetzung | PONS
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Übersetzung Englisch-Deutsch für thomas sebastian byrne im PONS Online-Wörterbuch nachschlagen! Gratis Vokabeltrainer, Verbtabellen, Aussprachefunktion.
Janine Wagenstaller
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Janine Wagenstaller. Details · Publications ... Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz-Depiereux, Bernd Kazmierczak, more · The American ...
Elisabeth Graf riemann - Traduction allemand-anglais | PONS
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Consultez la traduction allemand-anglais de Elisabeth Graf riemann dans le dictionnaire PONS qui inclut un entraîneur de vocabulaire, les tableaux de...
Academic Articles | FOXP1 Foundationwww.foxp1.org › academic-articles
www.foxp1.org
... Bettina Lorenz Depiereux, Sebastian Eck, Maja Hempel, Janine Wagenstaller, Alex Gawthrope, Anthony P Monaco, Michael Bonin, Olaf Riess, Eva Wohlleber, ...
Identification of FOXP1 deletions in three unrelated patients with...
healthdocbox.com
1 Identification of FOXP deletions in three unrelated patients with mental retardation and significant speech and language deficits Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, Ute Moog, Bettina Lorenz-Depiereux, Sebastian Eck, Maja Hempel, Janine Wagenstaller, Alex Gawthrope, Anthony P Monaco, et al.
Copy-Number Variations Measured by Single-Nucleotide ...www.academia.edu › Copy-Number_Variations_Me...
www.academia.edu
ARTICLE Copy-Number Variations Measured by Single-Nucleotide– Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation Janine Wagenstaller, ...
Gale OneFile: Health and Medicine - Document - DMP1 mutations in...
go.gale.com
Author(s): Bettina Lorenz-Depiereux [1, 12]; Murat Bastepe [2, 12]; Anna Benet-Pagès [1]; Mustapha Amyere [3]; Janine Wagenstaller [1]; Ursula Müller-Barth [4]; ...
Copy-number variations measured by single-nucleotide PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Janine Wagenstaller , Stephanie Spranger, Bettina Lorenz-Depiereux, Bernd Kazmierczak, Michaela Nathrath, Dagmar Wahl, Babett Heye, Dieter Glaser, ...
DMP1 mutations in autosomal recessive hypophosphatemia implicate a...
scholar.harvard.edu
Bettina Lorenz-Depiereux, Murat Bastepe, Anna Benet-Pagès, Mustapha Amyere, Janine Wagenstaller, Ursula Müller-Barth, Klaus Badenhoop, Stephanie M Kaiser,...
DMP1 mutations in autosomal recessive hypophosphatemia ...pubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Authors · Bettina Lorenz-Depiereux · Murat Bastepe · Anna Benet-Pagès · Mustapha Amyere · Janine Wagenstaller · Ursula Müller-Barth · Klaus Badenhoop · Stephanie M ...
Verwandte Suchanfragen zu Janine Wagenstaller
Klaus Badenhoop Olaf Riess Mustapha Amyere | Gertrud Eckstein Michael Bonin Bernd Kazmierczak | Michaela Nathrath Dagmar Wahl Denise Horn |
Personen Vorname "Janine" (15340) Name "Wagenstaller" (18) |
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