1
0
0
News
Vorstand und Organisation | agkgp-aktuell.de
agkgp-aktuell.de
Dr. Johannes Lemke, Leipzig. Prof. Dr. Andreas Tzschach, Freiburg. Dr. Katalin Komlosi, Freiburg (Wissenschaftliche Ko-Leitung des 23. Symposiums, Mai 2021) ...
Bücher
JIMD Reports - Case and Research Reports, Google Books
books.google.co.uk
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously...
JIMD Reports - Case and Research Reports, books.google.se › books
books.google.se
DOI _2012_187 CASE REPORT Katalin Komlósi • Anita Maa ́sz • Péter Kisfali • Kinga Hadzsiev • Judit Bene • Béla I. Melegh • Mária Ablonczy ...
Analysis of mtDNA A3243G mutation frequency in Hungary in ...www.degruyter.com › view › med....
www.degruyter.com
Aniko Gal , Katalin Komlosi , Anita Maasz , Klara Pentelenyi , Viktoria Remenyi , Csaba Ovary , Attila Valikovics , Peter Dioszeghy , Daniel Bereczki , Bela ...
Dokumente zum Namen
Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and...
www.scienceopen.com
Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome. Authors: Katalin Komlosi, Balazs Duga, Kinga Hadzsiev … See all cited by ...
EBSCOhost | | Deletion of 4q in the background of...
web.a.ebscohost.com
hypertension. Balazs Duga. 1,2. . Marta Czako. 1,2. . Katalin Komlosi. 1,2. .
EBSCOhost | | Protein tyrosine phosphatase gene C1858T...
web.b.ebscohost.com
Bernadett Farago · Gabor C. Talian · Katalin Komlosi · Gergely Nagy · Timea Berki ·. Agnes Gyetvai · Zoltan Szekanecz · Zoltan Nyarady ...
Wissenschaftliche Veröffentlichungen
Kleefstra syndrome in Hungarian patients: additional symptoms besides...
molecularcytogenetics.biomedcentral.com
... symptoms besides the classic phenotype. Kinga Hadzsiev,; Katalin Komlosi,; Marta Czako,; Balazs Duga,; Renata Szalai,; Andras Szabo,; Etelka Postyeni,; Titanilla Szabo,; Gyorgy Kosztolanyi and; Bela MeleghEmail author. Molecular Cytogenetics20169:22. https://doi.org s
FreiDok plus - Komlosi, Katalin
freidok.uni-freiburg.de
Katalin Komlosi. Seit. Beschreibung. Forschungsschwerpunkte. Diese Person in anderen Informationssystemen. GND-Nummer ORCID iD ...
Johannes Gutenberg Universität
jogustine.uni-mainz.de
Dr. Oliver Bartsch; Prof. Dr. Susann Schweiger; PD Dr. Ulrich Zechner; Dr. Katalin Komlosi. Event type: Lecture. Displayed in timetable as: Vl: Humangenetik.
Veröffentlichungen allgemein
Phenotypic variability in a Hungarian patient with the 4q Core
core.ac.uk
All authors read and approved the final manuscript. Authors' information. Katalin Komlosi and Balazs Duga both should be considered 1st authors. Komlósi et al.
User blog:Just Dance Now Users/Just Dance Now (Katalin Komlosi) |...
justdance.fandom.com
Aserejé (The Ketchup Song) Beware of the Boys (Mundian To Bach Ke)
Does glycoprotein IIIa gene (Pl(A)) polymorphism influence...
www.wikidata.org
3. 0 references. Katalin Komlosi. series ordinal references. Gabor Talian. series ordinal references. Gergely Feher. series ordinal. 6.
Sonstiges
Fallpräsentation Fall 1: Sven Klimpe, Stefan Klebe , Katalin Komlosi...
slideplayer.org
Anamnese / Fremdanamnese / Verlauf Fall 1 Anamnese / Fremdanamnese / Verlauf Anamnese incl. Vorgeschichte 37jähriger Patient, unauffällige, zeitgerechte...
Dr. med. Katalin Komlosi in Mainz FA für Humangenetik - aerzte...
www.aerzte.de
➤ Dr. med. Katalin Komlosi in Mainz FA für Humangenetik ➤ Bewertungen, Leistungen, Telefonnummern, Öffnungszeiten, Online Wunsch-Termin ➤ Jetzt klicken!
Katalin Komlosi - PSJD - Yadda
psjd.icm.edu.pl
Copy. Full name. Katalin Komlosi. Surname. Komlosi. Forename. Katalin. Roles. author (search). Address. Contact information. ICM UW · Centrum otwartej nauki
(PDF) Mitochondrial DNA C>A Mutation Associated Leigh Syndrome:...
www.academia.edu
Mitochondrial DNA C>A Mutation Associated Leigh Syndrome: Case Report with a Review of the Previously Described Pedigrees
Tag der Seltenen Erkrankungen in Mainz
de-de.fievent.com
Programm 9:00 – 13:10 Uhr Selbsthilfegruppen und Verein..., Freitag, 03. März 2017, Mainz
Analysis of mtDNA A3243G mutation frequency in Hungary - Open...
psjd.icm.edu.pl
Aniko Gal , Katalin Komlosi , Anita Maasz , Klara Pentelenyi , Viktoria Remenyi , Csaba Ovary , Attila Valikovics , Peter Dioszeghy , Daniel Bereczki , Bela ...
Humangenetiker in Wiesbaden, Hessen bei ärzte.de - Hier den richtigen...
www.aerzte.de
➤ Hier finden Sie den richtigen Humangenetiker in Wiesbaden, Hessen! ➤ 12 Ärzte mit Bewertungen, Leistungen, Öffnungszeiten, Einfach Online Wunsch-Termin ➤...
Altmetric – Partial tetrasomy of the proximal long arm of chromosome...
www.altmetric.com
... Duga, Balazs, Komlosi, Katalin, Melegh, Bela, Andras Szabo, Marta Czako, Kinga Hadzsiev, Balazs Duga, Katalin Komlosi, Bela Melegh.
Altmetric – Kleefstra syndrome in Hungarian patients: additional...
www.altmetric.com
Kinga Hadzsiev, Katalin Komlosi, Marta Czako, Balazs Duga, Renata Szalai, Andras Szabo, Etelka Postyeni, Titanilla Szabo, Gyorgy Kosztolanyi, Bela Melegh.
Glycoprotein IIIA (PlA) polymorphism aspirin resistance: Is there any...
experts.umn.edu
Elod Papp, Viktoria Havasi, Judit Bene, Katalin Komlosi, Laszlo Czopf, Eva Magyar, Csaba Feher, Gergely Feher, Beata Horvath, Zsolt Marton, ...
Phenotypic Variants of the Deafness-Associated Mitochondrial DNA...
www.eurekaselect.com
A number of nuclear and mitochondrial mutations have been implicated in non-syndromic hearing loss. Among them, various mutations of mitochondrial SerUCN-t
Kleefstra syndrome in Hungarian patients: additional symptoms besides...
real.mtak.hu
Depositing User: Dr. Katalin Komlosi. Date Deposited: 02 Oct :43. Last Modified: 02 Oct :43. URI: http://real.mtak.hu/id/eprint
Deletion of 4q in the background of multiple malformations...
real.mtak.hu
Depositing User: Dr. Katalin Komlosi. Date Deposited: 23 Sep :06. Last Modified: 23 Sep :06. URI: http://real.mtak.hu/id/eprint
SciELO - Brazil - The Role of Next-Generation Sequencing in the...
www.scielo.br
The Role of Next-Generation Sequencing in the Diagnosis of Lysosomal Storage Disorders. Katalin Komlosi. Alexander Sólyom. Michael Beck.
141 "Komlosi" names Agnes Komlosi...
child-names.com
Katalin Komlosi. Jozef Komlosi. Istvan Komlosi. Ioan Komlosi. Ilona Komlosi. Ildi Komlosi. Gyongyi Komlosi. Gergely Komlosi. Gabriel Komlosi. Gabi Komlosi.
Tag der Seltenen Erkrankungen in Mainz | Event | Mainz
de.eventbu.com
Tag der Seltenen Erkrankungen in Mainz im Mainz, Mainzer Rathaus, Freitag, 03. März Programm 9:00 – 13:10 Uhr Selbsthilfegruppen und Vereine beraten und...
Kleefstra syndrome in Hungarian patients: additional symptoms besides...
go.gale.com
includes Kleefstra syndrome in Hungarian patients: additional sy by Kinga Hadzsiev, Katalin Komlosi, Marta . Click to explore.
Targeted next-generation sequencing analysis in couples at increased...
pubmed.ncbi.nlm.nih.gov
For the families in whom causative variants could be identified, these may now be used for prenatal and preimplantation genetic diagnostics. Our data show that...
Tanítványaimban élek tovább · Erdős Katalin – Komlósi Éva (szerk.) ·...
moly.hu
Tanítványaimban élek tovább 0 csillagozás. Emlékkötet Buday-Sántha Attila tiszteletére. Erdős Katalin – Komlósi Éva (szerk.): Tanítványaimban élek tovább.
Targeted next-generation sequencing analysis in couples at increased...
medworm.com
Many of the genetic childhood disorders leading to death in the pre- or neonatal period or during early childhood follow autosomal recessive modes of...
Verwandte Suchanfragen zu Katalin Komlosi
| Bela Melegh Peter Dioszeghy Andras Szabo | Daniel Bereczki |
Personen Vorname "Katalin" (1123) Name "Komlosi" (13) |
sortiert nach Relevanz / Datum