Affiner les résultats
Type de document
Institution
Collection spécifique
Langue
- Anglais (21)
Auteur
- Nürnberg, Peter (5)
- Altmüller, Janine (4)
- Thiele, Holger (4)
- Basel-Vanagaite, Lina (2)
- Beleggia, Filippo (2)
- Hildebrandt, Friedhelm (2)
- Nürnberg, Gudrun (2)
- Pasch, Andreas (2)
- Rauch, Anita (2)
- Steindl, Katharina (2)
- Wollnik, Bernd (2)
- Zweier, Christiane (2)
- Abdel-Salam, Ghada (1)
- Abdenur, Jose (1)
- Al Jasmi, Fatma (1)
- Alanay, Yasemin (1)
- Albrecht, Beate (1)
- Alexov, Emil (1)
- Ansar, Muhammad (1)
- Anyane-Yeboa, Kwame (1)
- Arrigoni, Eviano (1)
- Ashraf, Shazia (1)
- Attanasio, Massimo (1)
- Avanzini, Giuliano (1)
- Baasner, Anne (1)
- Baig, Shahid M. (1)
- Balemans, Wendy (1)
- Ballhausen, D. (1)
- Balschun, Tobias (1)
- Baltsavias, Gerasimos (1) Plus Moins
Mot clé
- Adaptation (1)
- Arterio-venous fistula (1)
- Dural sinus malformation (1)
- Exome (1)
- Familial adenomatous polyposis (1)
- GH (1)
- GHR gene mutation (1)
- Hereditary colorectal cancer (1)
- Hereditary disease (1)
- Hereditary nonpolyposis colorectal cancer (1)
- IGF-I (1)
- Institute of Medical Genetics (1)
- Langer-Giedion syndrome (1)
- Microsatellite instability (1)
- Mismatch repair (1)
- Mutation (1)
- Nucleic Acid Enzymes (1)
- Original Articles (1)
- Polymorphism (1)
- Rht8 (1)
- Tricho-rhino-phalangeal disease type II (1)
- brassinosteroid (1)
- congenital anomalies of the kidney and urinary tract (CAKUT) (1)
- desmin-related myopathy (1)
- desminopathy (1)
- height (1)
- idiopathic short stature (1)
- kidney development (1)
- myofibrillar myopathy (1)
- scapuloperoneal syndrome (1) Plus Moins