Institute of Human Genetics - University Hospital of Cologne, Germany

<body> <h2>Institute of Human Genetics Cologne, Germany</h2> <p>This Web Site needs Javascript for representation and navigation. Please activate Javascript in your Browser.</p> <p>Should you visit us with an ASCII-Browser, then please try to select directly the desired information from the following overview.</p> <p>Please note, that not all information can be represented correctly without Javascript and graphical Browser.</p> <p><strong>Director:</strong> <br> Prof. Dr. Brunhilde Wirth</p> <p align="left"><strong>Head of Genetic Counselling Services:</strong> <br> Prof. Dr. Christian Kubisch</p> <p><strong>Senior Clinical Geneticist:</strong> <br> Dr. Raoul Heller, PhD</p> <p><strong>Clinical Geneticists:</strong> <br> Dr. med. Guntram Borck<br /> PD Dr. med. Christian Netzer (Leader of the Human Genetics Section of <a href="mvz/index.en.html" target="_self">MVZ</a>) <br> Dr. med. Alexander Volk Dr. med. Bernd Wollnik<br />        (Leader of Junior Research Group, <a href="http://www.zmmk.uni-koeln.de" target="_blank">ZMMK</a>)</p> <p><strong>Molecular genetic testing:</strong><br /> Dr. Anne Baasner<br> Dr. Jutta Becker</p> <p><strong>Secretary to Prof. Wirth:</strong> Dr. Uwe Becker<br> <strong>Secretary of Genetic Counselling Services:</strong><br> Karin Boß </p> <p><strong>IT Manager und Webmaster:</strong><br /> Dr. Radu Wirth (Medical Informatics)</p> <p><strong>Address</strong>: <br> Institute of Human Genetics<br> University Hospital of Cologne<br> Building 47, 9th floor<br> Kerpener Str. 34<br> D - 50931 Cologne<br> Germany </p> <p align="left"><strong>Secretary to Prof. Wirth</strong><br> Phone: ++49-(0)221-478-86464<br> Fax: ++49-(0)221-478-86465</p> <p align="left"><strong>Genetic Counselling Services<br> </strong>Phone: ++49-(0)221-478-86811<br> Fax: ++49-(0)221-478-86812</p> <p align="left"><b><strong>Laboratories</strong> :</b><br> <b><a href="http://www.genetik.uni-koeln.de" target="_blank">Institute of Genetics</a></b> of <a href="http://www.uni-koeln.de" target="_blank">University of Cologne</a><br> Zülpicher Str. 47, 50674 Cologne (1. floor)<br> Contact: <a href="mitarbeiter/liste/index.en.html">Staff, List</a></p> <p align="left"><b>CMMC - Center for Molecular Medicine, University of Cologne (ZMMK)</b><br> Robert-Koch-Str. 21, 50931 Cologne<br> Contact: <a href="mitarbeiter/liste/index.en.html">Staff, List</a><br> <p align="left"> </p> <p align="left"><a href="index_frames.html">Home, Hauptseite mit Frames, deutsch/ german home page, Entry, Main page with Frames </a></p> <p align="left"> </p> <p><a href="beratung/info_allg/index.en.html">General Informations: Genetic counseling at the Institute of Human genetics Cologne Germany </a></p> <p><a href="beratung/info_pat/index.en.html">Information for patients and interested persons: Informations about selected genetic disorders/ diseases </a></p> <p><a href="diagnostik/formulare/index.en.html">Forms for genetic testing at the Institute of Human genetics Cologne Germany</a></p> <p><a href="diagnostik/haut/ichthyosis/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Skin: Autosomal Recessive Congenital Ichthyosis (ARCI, LI, NCIE)</a></p> <p><a href="diagnostik/herz_kreis/cmd1a/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Cardiovascular disorders: Dilated Cardiomyopathy with Conduction Defect (CMD1A, CDCD1)</a></p> <p><a href="diagnostik/herz_kreis/leopard/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Cardiovascular disorders: LEOPARD Syndrome; Progressive Cardiomyopathic Multiple Lentiginosis Syndrome</a></p> <p><a href="diagnostik/herz_kreis/lqts/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Cardiovascular disorders: Long QT Syndrome (LQTS), Romano-Ward Syndrome (RWS), Jervell and Lange-Nielsen Syndrome (JLNS)</a></p> <p><a href="diagnostik/herz_kreis/noonan/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Cardiovascular disorders: Noonan Syndrome Type 1 (NS1)</a></p> <p><a href="diagnostik/neuromusk/als/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Neuromuscular disorders: Amyotrophic Lateral Sclerosis (ALS), Lou Gehrig’s Disease</a></p> <p><a href="diagnostik/neuromusk/sma/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Neuromuscular disorders: Spinal Muscular Atrophy, autosomal recessive, proximal (SMA)</a></p> <p><a href="diagnostik/neuromusk/smard/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Neuromuscular disorders: Infantile spinal muscular atrophy with respiratory distress, type 1 (SMARD1)</a></p> <p><a href="diagnostik/seh_hoer/adrp/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Eye and hearing disorders: Autosomal Dominant Retinitis Pigmentosa (ADRP)</a></p> <p><a href="diagnostik/seh_hoer/dfnb/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Eye and hearing disorders: Autosomal Recessive Hearing Loss (DFNB1; Connexin 26 and Connexin 30)</a></p> <p><a href="diagnostik/seh_hoer/ush2/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Eye and hearing disorders: Usher Syndrome Type 2 (USH2)</a></p> <p><a href="diagnostik/skelett/da/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Skeletal dysplasia: Distal Arthrogryposis multiplex congenita (DA), Type 1 and 2(A/)B</a></p> <p><a href="diagnostik/skelett/opd/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Skeletal dysplasia: OPD Spectrum Disorders (Filamin A), otopalatodigital syndrome type 1 or 2 (OPD1/2), Melnick-Needles syndrome (MNS), frontometaphyseal dysplasia (FMD)</a></p> <p><a href="diagnostik/niere/hyperoxalurie/index.en.html">Clinical diagnostics, Diagnostic investigation, genetic testing: Kidney disorders: Primary Hyperoxaluria Type I and Type II (HP I and II) (AGXT, GRHPR)</a></p> <p><a href="forschung/bericht/projekte.en.html">Research, Reports, Projects</a></p> <p><a href="forschung/bericht/publikationen.en.html">Research, Reports, Publications</a></p> <p><a href="forschung/bericht/diplome.en.html">Research, Reports, Diploma-, Bachelor-, Master- Thesis</a></p> <p><a href="forschung/bericht/promotionen.en.html">Research, Reports, doctoral thesis, dissertations</a></p> <p><a href="forschung/bericht/habil.en.html">Research, Reports, postdoctoral lecture qualifications </a></p> <p><a href="forschung/bolz/index.en.html">Research: Work Group Bolz</a></p> <p><a href="forschung/hahnen/index.en.html">Research: Work Group Hahnen</a></p> <p><a href="forschung/kubisch/index.en.html">Research: Work Group Kubisch</a></p> <p><a href="forschung/wirth/index.en.html">Research: Work Group Wirth</a></p> <p><a href="forschung/wirth/carnival.en.html">CARNI-VAL: International clinical Study on SMA Typ I started 09/25/2009</a></p> <p><a href="forschung/wollnik/index.en.html">Research: Work Group Wollnik</a></p> <p><a href="impressum/index.en.html">Legal Notices, Impressum</a></p> <p><a href="institut/kontakt/index.en.html">Institute of Human Genetics Cologne, Germany, Contact, Address, Phone, Fax</a></p> <p><a href="institut/standort/frauenklinik.en.html">Institute of Human Genetics Cologne, Germany, Location in the Obstetrics and Gynaecology - Building (Frauenklinik)</a></p> <p><a href="institut/standort/zmmk.en.html">Institute of Human Genetics Cologne, Germany, Location CMMC - Center for Molecular Medicine, University of Cologne (ZMMK) </a></p> <p><a href="institut/standort/genetik.en.html">Institute of Human Genetics Cologne, Germany, Location at the Institute of Genetics</a></p> <p><a href="institut/wir/index.en.html">Institute of Human Genetics Cologne, Germany, Introducing ourselves</a></p> <p><a href="mvz/index.en.html">Medizinisches Versorgungszentrum der Uniklinik Köln am Neumarkt (MVZ)</a></p> <p><a href="lehre/uebersicht/hg_lehre.0910ws.en.pdf">Teaching, Synopsis</a></p> <p><a href="lehre/diplom/index.en.html">Teaching, Degree, Theses</a></p> <p><a href="lehre/klausuren/index.en.html">Teaching, Tests</a></p> <p><a href="termine/kolloquium/index.en.html">Teaching Colloquium, see Events, Colloquium</a></p> <p><a href="lehre/praktika/medizin.en.html"> Teaching, Practical Courses, Medical Students</a></p> <p><a href="lehre/praktika/biologie.en.html">Teaching, Practical Courses, Biology Students</a></p> <p><a href="lehre/seminare/index.en.html">Teaching, Seminars</a></p> <p><a href="lehre/vorlesungen/index.en.html">Teaching, Courses</a></p> <p><a href="lehre/kompetenzfelder/erbkrankheiten/index.en.html">Teaching, Fields of Expertise, Inherited Diseases</a></p> <p><a href="lehre/kompetenzfelder/schwangerschaft/index.en.html">Teaching, Fields of Expertise, Pregnancy</a></p> <p><a href="lehre/scheinausgabe/index.en.html">Teaching, Issue of Certificates</a></p> <p><a href="lehre/literatur/index.en.html">Teaching, Recommended Literature</a></p> <p><a href="links/index.en.html">Human Genetics - Links</a></p> <p><a href="mitarbeiter/liste/index.en.html">Staff, List</a></p> <p><a href="stellen/index.en.html">Jobs</a></p> <p><a href="termine/kolloquium/index.en.html">Events, Colloquium</a></p> <p><a href="termine/tagung_kongress/index.en.html">Events, Meetings / Congresses</a></p> <p><a href="weiterbildung/fahg/index.en.html">Professional Training, Clinical Geneticist</a></p> <p><a href="weiterbildung/fhg/index.en.html">Professional Training, Human Geneticist</a></p> <p><a href="hinweis.en.html">Important Information</a></p> <p><a href="forschung/wirth/pmid_18440926.en.html">NEWS/Science: Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy - How the modified expression of a gene compensates the loss of another gene: Plastin 3 protects against SMA</a></p> <p>WEB-Master: Dr. Radu Wirth</p> </body>