AAAAAA

   
Results: 1-4 |
Results: 4

Authors: DEBOO GM TIBBEN A LANSER JBK JENNEKENSSCHINKEL A HERMANS J MAATKIEVIT A ROOS RAC
Citation: Gm. Deboo et al., EARLY COGNITIVE AND MOTOR SYMPTOMS IN IDENTIFIED CARRIERS OF THE GENEFOR HUNTINGTON-DISEASE, Archives of neurology, 54(11), 1997, pp. 1353-1357

Authors: HORSTHEMKE B MAATKIEVIT A SLEEGERS E VANDENOUWELAND A BUITING K LICH C MOLLEVANGER P BEVERSTOCK G GILLESSENKAESBACH G SCHWANITZ G
Citation: B. Horsthemke et al., FAMILIAL TRANSLOCATIONS INVOLVING 15Q11-Q13 CAN GIVE RISE TO INTERSTITIAL DELETIONS CAUSING PRADER-WILLI OR ANGELMAN SYNDROME, Journal of Medical Genetics, 33(10), 1996, pp. 848-851

Authors: SCHRANDERSTUMPEL C MEINECKE P WILSON G GILLESSENKAESBACH G TINSCHERT S KONIG R PHILIP N RIZZO R SCHRANDER J PFEIFFER L MAATKIEVIT A VANDERBURGT I VANESSEN T LATTA E HILLIG U VERLOES A JOURNEL H FRYNS JP
Citation: C. Schranderstumpel et al., THE KABUKI (NIIKAWA-KUROKI) SYNDROME - FURTHER DELINEATION OF THE PHENOTYPE IN 29 NON-JAPANESE PATIENTS, European journal of pediatrics, 153(6), 1994, pp. 438-445

Authors: MAATKIEVIT A BRUNNER HG MAASWINKELMOOIJ P
Citation: A. Maatkievit et al., 2 ADDITIONAL CASES OF THE OHDO BLEPHAROPHIMOSIS SYNDROME, American journal of medical genetics, 47(6), 1993, pp. 901-906
Risultati: 1-4 |