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Research Roundtable - Peter Gergics | Human Genetics | Michigan...
medicine.umich.edu
Research Roundtable - Peter Gergics. 12:00 PM Buhl Peter Gergics, M.D., Ph.D. Research Investigator of Human Genetics Home; Graduate …
Telephone & Addresses
WhitePages: 3631 Bent Trail Dr, Ann Arbor, MI | Whitepageswww.whitepages.com › ... › MI › Ann Arbor ›
Bent Trail Dr. Dawn Fleshman, Jia J Liu, David William Armstrong · Meadow Grove Trl. Peter Gergics, Mary M Moeller, Edgar Allen Knight I.
Network Profiles
LinkedIn: Peter Gergics | LinkedIn
Peter Gergics’ berufliches Profil anzeigen LinkedIn ist das weltweit größte professionelle Netzwerk, das Fach- und Führungskräften wie Peter Gergics dabei hilft ...
Search Results - Endocrine Society
press.endocrine.org
Peter Gergics, Helen C. Christian, Monica S. Choo ... Please login to be able to save your searches and receive alerts for new content matching your search criteria ...
Grant Mastick | Molecular Biosciences Graduate Programs Faculty |...
www.unr.edu
Kyung-Tai Kim, Namhee Kim, Hwan-Ki Kim, Hojae Lee, Peter Gergics, Chungoo Park, Hannah N. Gruner, Grant S. Mastick, Hae-Chul Park, and Mi-Ryoung ...
Books & Literature
Endocrine Gland Development and Diseasebooks.google.com › books
books.google.de
... Arbor, Michigan, USA Peter Gergics Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA Elisabet Gjernes Univ.
Genetics of Endocrine Diseases and Syndromesbooks.google.com › books
books.google.de
Peter Gergics Abstract Congenital pituitary hormone deficiency is a disabling condition. It is part of a spectrum of disorders including craniofacial midline ...
Related Documents
HRWC-AnnualReport SlideSharewww.slideshare.net › ElizabethRiggs › hrwcannualrepo...
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... Connor Genther Daniel Gergics Lilla Gergics Peter Gergics Eliana Ginis Zachery Gizicki David Goddard David Goodman Robert Goodspeed ...
CiteSeerX — gene in an extended
citeseerx.ist.psu.edu
BibTeX @MISC{Patocs08genein, author = {Attila Patocs and Peter Gergics and Katalin Balogh and Miklos Toth and Ferenc Fazakas and Istvan Liko and Karoly Racz}, title
BMC Endocrine Disorders reviewer acknowledgement library.net › Other
1library.net
Neetika Garg. United States of America. Erica Gentilin Italy. Peter Gergics. United States of America. Laura Gianotti Italy. Oliver Gimm Sweden.
Publications Attila Patócs MD, MSc, PhD
www.bel2.semmelweis.hu
Peter Gergics, Attila Patocs, Miklos Toth, Peter Igaz, Nikolette Szucs, Istvan Liko, Ferenc Fazakas, Istvan Szabo, Balazs Kovacs, Edit Glaz, Karoly Racz: Germline
Scientific Publications
Gene Expression in Mouse Thyrotrope Adenoma PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Authors. Peter Gergics , Helen C Christian , Monica S Choo , Adnan Ajmal , Sally A Camper. Affiliation. 1 Department of Human Genetics (P.G., M.S.C., S.A.C.), ...
Endocrine gland development and disease - NLM Catalog - NCBI
www.ncbi.nlm.nih.gov
Catalog of books, journals, and audiovisuals at the National Library of Medicine.
BMC Developmental Biology | Articles
bmcdevbiol.biomedcentral.com
BMC Developmental Biology is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across...
Novel mutation of the CYP17 gene in two unrelated patients ...pubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Attila Patocs , István Liko, Ibolya Varga, Peter Gergics, Andras Boros, Laszlo Futo, Imre Kun, Rita Bertalan, Szilvia Toth, Tamas Pazmany, Miklós Toth, Nikolette ...
Publications
Publications Authored by Peter Gergics | PubFacts
www.pubfacts.com
Publications Authored by Peter Gergics
Current topics in developmental biology. Volume one hundred and six,...
www.worldcat.org
Diesen Titel erhalten Sie in einer Bibliothek! Current topics in developmental biology. Volume one hundred and six, Endocrine gland development and disease....
Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene...
www.oalib.com
Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau ... Attila Patocs, Peter Gergics, Katalin Balogh ...
BMC Medical Genetics - oalib
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OA Library offers high quality and most updated free academic thesis,open access resource covering various fields.It also provides Comprehensive Research Tool.
Miscellaneous
Peter Gergics | LinkedIn
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View Peter Gergics’ professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Peter Gergics discover inside ...
Peter Gergics, Medical Student in Ypsilanti - NPI ,...
npino.com
NPI Peter Gergics, Medical Student in Ypsilanti - Practice Location Address, Taxonomy and Contact
Peter Gergics, MD, PhD
endo.confex.com
Peter Gergics, MD, PhD. University of Michigan Human Genetics Papers: OR17-2 Thyrotrope Adenoma Mouse Model Exhibits Altered Expression of Multiple …
Gergics - Names Encyclopedia
namespedia.com
Peter Gergics (1) Matyas Gergics (1) Istvanne Gergics (1) Bernadett Gergics (1) Bertalan Gergics (1) Belane Gergics (1) Aranka Gergics (1) Antal Gergics (1)
BMC Medical Genetics BioMed Central - unideb.hu
dea.lib.unideb.hu
BMC Medical Genetics Research article Open Access ... Attila Patocs1, Peter Gergics 2, Katalin Balogh , Miklos Toth 2, Ferenc Fazakas 3, Istvan Liko4 and Karoly Racz*2
ISS3 - endo.confex.com
endo.confex.com
Peter Gergics, MD PhD, Human Genetics, University of Michigan, Ann Arbor, MI Nothing to Disclose: PG 8:20 AM. 1SS3-2. Practical Issues for International Clinicians ...
(PDF) Germline VHL gene mutations in Hungarian families with von...
www.academia.edu
Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas
All figures were generated with Swiss-PdbViewer in Figsharefigshare.com › articles › figure › All_figures_were_gen...
figshare.com
posted on , 08:50 by Attila Patocs, Peter Gergics, Katalin Balogh, Miklos Toth, Ferenc Fazakas, Istvan Liko, Karoly Racz. Copyright information:.
(PDF) MEN1 gene mutations in Hungarian patients with multiple...
www.academia.edu
MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1
Germline VHL gene mutations in Hungarian families with von...
eje.bioscientifica.com
Germline VHL gene mutations in Hungarian families with von Hippel–Lindau disease and patients with apparently sporadic unilateral pheochromocytomas Peter Gergics,
PubPeer - The pattern of congenital heart defects arising from...
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PubPeer enables scientists to search for their publications or their peers publications and provide feedback and/or start a conversation anonymously.
BioKDEbiokde.com › doc
biokde.com
Peter Gergics, Michelle L Brinkmeier, Sally A Camper +7 authors, Hwan-Ki Kim, Hojae Lee, Hannah N Gruner, Peter Gergics, Chungoo Park, Grant S Mastick, ...
ISL1-based LIM complexes control Slit2 transcription in developing...
koreauniv.pure.elsevier.com
Kyung Tai Kim, Namhee Kim, Hwan Ki Kim, Hojae Lee, Hannah N. Gruner, Peter Gergics, Chungoo Park, Grant S. Mastick, Hae Chul Park, ...
Lhx4 deficiency: increased cyclin-dependent kinase inhibitor ...accounts.public.ce.basespace.illumina.com › article
accounts.public.ce.basespace.illumina.com
Peter Gergics, Michelle L Brinkmeier, Sally A Camper. Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.
March in preprints - the Nodethenode.biologists.com › highlights
thenode.biologists.com
... Kiseleva, Audrey C.A. Cleuren, Kart Tomberg, Martijn A. van der Ent, Peter Gergics, K. Sue O Shea, Thomas L. Saunders, David Ginsburg.
Papers in the shared collection Short stature | Read by QxMDread.qxmd.com › shared-collection
read.qxmd.com
Qing Fang, Akima S George, Michelle L Brinkmeier, Amanda H Mortensen, Peter Gergics, Leonard Y M Cheung, Alexandre Z Daly, Adnan Ajmal, María Ines ...
Residents | Internal Medicine Residency | St. Joseph Mercy ...www.stjoeshealth.org › ... › Residents › Current Residents
www.stjoeshealth.org
Peter Gergics, MD. School: Semmelweis University - Hungary Hometown: Kecskemet, Hungary Hobbies/interests: Spending time with my kids, cooking, archery, ...
SAT-291 SIX3 Is Essential for Hypothalamic and Pituitary Development...
academic.oup.com
Abstract. The genetic basis for congenital hypopituitarism and related disorders is beginning to emerge, and over causal 30 genes have been identified, includin
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... Peter Gergics, Virginia Pesch, Shigeki Iwase, Ryan E. Mills, Devika Bagchi, Yifan Wang, Sierra Nishizaki, Arushi Varshney, Barbara S. Nelson, Weichen Zhou, ...
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