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1. VANDERBURGT I; THOONEN G; ASSMANHULSMANS C; BRUNNER H; GABREELS F; OTTEN B
   PATTERNS OF COGNITIVE-FUNCTIONING IN SCHOOL-AGED CHILDREN WITH NOONAN-SYNDROME ASSOCIATED WITH THE VARIABILITY IN PHENOTYPICAL EXPRESSION
   European journal of human genetics
   
   I. Vanderburgt et al., "PATTERNS OF COGNITIVE-FUNCTIONING IN SCHOOL-AGED CHILDREN WITH NOONAN-SYNDROME ASSOCIATED WITH THE VARIABILITY IN PHENOTYPICAL EXPRESSION", European journal of human genetics, 6, 1998, pp. 1031-1031
2. KREMER H; CROSBY AH; VANREEN M; KENMOCHI N; ION A; JAMIESON CR; VANDERBURGT I; PATTON MA; MARIMAN ECM; JEFFERY S
   EXCLUSION OF THE MYOSIN LIGHT-CHAIN-2 GENE AND THE RIBOSOMAL-PROTEIN L6 GENE FROM A CAUSATIVE ROLE IN THE PATHOGENESIS OF NOONAN-SYNDROME
   European journal of human genetics
   
   H. Kremer et al., "EXCLUSION OF THE MYOSIN LIGHT-CHAIN-2 GENE AND THE RIBOSOMAL-PROTEIN L6 GENE FROM A CAUSATIVE ROLE IN THE PATHOGENESIS OF NOONAN-SYNDROME", European journal of human genetics, 6, 1998, pp. 4184-4184
3. WIJMENGA C; VANDENHEUVEL L; STRENGMAN E; LUYTEN J; VANDERBURGT I; DEGROOT R; SMEETS D; VANDONGEN J; PEARSON P; SANDKUIJL L; WEEMAES C
   LOCALIZATION OF ICF SYNDROME BY HOMOZYGOSITY MAPPING
   Molecular immunology
   
   C. Wijmenga et al., "LOCALIZATION OF ICF SYNDROME BY HOMOZYGOSITY MAPPING", Molecular immunology, 35(11-12), 1998, pp. 719-719
4. POLINKOVSKY A; ROBIN NH; THOMAS JT; IRONS M; LYNN A; GOODMAN FR; REARDON W; KANT SG; BRUNNER HG; VANDERBURGT I; CHITAYAT D; MCGAUGHRAN J; DONNAI D; LUYTEN FP; WARMAN ML
   MUTATIONS IN CDMP1 CAUSE AUTOSOMAL-DOMINANT BRACHYDACTYLY TYPE-C
   Nature genetics
   
   A. Polinkovsky et al., "MUTATIONS IN CDMP1 CAUSE AUTOSOMAL-DOMINANT BRACHYDACTYLY TYPE-C", Nature genetics, 17(1), 1997, pp. 18-19
5. BRADY AF; JAMIESON CR; VANDERBURGT I; CROSBY A; VANREEN M; KREMER H; MARIMAN E; PATTON MA; JEFFERY S
   FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12
   European journal of human genetics
   
   A.F. Brady et al., "FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12", European journal of human genetics, 5(5), 1997, pp. 336-337
6. DESCHEPPER J; OTTEN BJ; FRANCOIS I; BOURGUIGNON JP; CRAEN M; VANDERBURGT I; MASSA GG
   GROWTH-HORMONE THERAPY IN PRE-PUBERTAL CHILDREN WITH NOONAN-SYNDROME - FIRST YEAR GROWTH-RESPONSE AND COMPARISON WITH TURNER-SYNDROME
   Acta paediatrica
   
   J. Deschepper et al., "GROWTH-HORMONE THERAPY IN PRE-PUBERTAL CHILDREN WITH NOONAN-SYNDROME - FIRST YEAR GROWTH-RESPONSE AND COMPARISON WITH TURNER-SYNDROME", Acta paediatrica, 86(9), 1997, pp. 943-946
7. ROBIN NH; POLINKOVSKY A; GUNAYAYGUN M; THOMAS JT; IRONS M; LYNN A; GOODMAN FR; REARDON W; KANT SG; BRUNNER HG; VANDERBURGT I; CHITAYAT D; MORRISON S; LUYTEN FP; WARMAN ML
   BRACHYDACTYLY TYPE-C IS CAUSED BY MUTATIONS IN THE MORPHOGEN CDMP-1
   American journal of human genetics
   
   N.H. Robin et al., "BRACHYDACTYLY TYPE-C IS CAUSED BY MUTATIONS IN THE MORPHOGEN CDMP-1", American journal of human genetics, 61(4), 1997, pp. 251-251
8. HAMEL BCK; RAAMS A; SCHUITEMADIJKSTRA AR; SIMONS P; VANDERBURGT I; JASPERS NGJ; KLEIJER WJ
   XERODERMA PIGMENTOSUM-COCKAYNE SYNDROME COMPLEX - A FURTHER CASE
   Journal of Medical Genetics
   
   B.C.K. Hamel et al., "XERODERMA PIGMENTOSUM-COCKAYNE SYNDROME COMPLEX - A FURTHER CASE", Journal of Medical Genetics, 33(7), 1996, pp. 607-610
9. VANDERBURGT I; CHRZANOWSKA KH; SMEETS D; WEEMAES C
   NIJMEGEN BREAKAGE SYNDROME
   Journal of Medical Genetics
   
   I. Vanderburgt et al., "NIJMEGEN BREAKAGE SYNDROME", Journal of Medical Genetics, 33(2), 1996, pp. 153-156
10. MULLIS PE; ARGENTE J; AMSELEM S; PFAFFLE R; VANDERBURGT I
    GENETICS AND MOLECULAR-BIOLOGY IN SHORT STATURE
    Acta paediatrica
    
    P.E. Mullis et al., "GENETICS AND MOLECULAR-BIOLOGY IN SHORT STATURE", Acta paediatrica, 84, 1995, pp. 75-80
11. SULISALO T; VANDERBURGT I; RIMOIN DL; BONAVENTURE J; SILLENCE D; CAMPBELL JB; CHITAYAT D; SCOTT CI; DELACHAPELLE A; SISTONEN P; KAITILA I
    GENETIC HOMOGENEITY OF CARTILAGE HAIR HYPOPLASIA
    Human genetics
    
    T. Sulisalo et al., "GENETIC HOMOGENEITY OF CARTILAGE HAIR HYPOPLASIA", Human genetics, 95(2), 1995, pp. 157-160
12. LIN AE; GORLIN RJ; LURIE IW; BRUNNER HG; VANDERBURGT I; NAUMCHIK IV; RUMYANTSEVA NV; STENGELRUTKOWSKI S; ROSENBAUM K; MEINECKE P; MULLER D
    FURTHER DELINEATION OF THE BRANCHIOOCULOFACIAL SYNDROME
    American journal of medical genetics
    
    A.E. Lin et al., "FURTHER DELINEATION OF THE BRANCHIOOCULOFACIAL SYNDROME", American journal of medical genetics, 56(1), 1995, pp. 42-59
13. JAMIESON CR; VANDERBURGT I; BRADY AF; VANREEN M; ELSAWI MM; HOL F; JEFFERY S; PATTON MA; MARIMAN E
    MAPPING A GENE FOR NOONAN-SYNDROME TO THE LONG ARM OF CHROMOSOME-12
    Nature genetics
    
    C.R. Jamieson et al., "MAPPING A GENE FOR NOONAN-SYNDROME TO THE LONG ARM OF CHROMOSOME-12", Nature genetics, 8(4), 1994, pp. 357-360
14. 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
    THE KABUKI (NIIKAWA-KUROKI) SYNDROME - FURTHER DELINEATION OF THE PHENOTYPE IN 29 NON-JAPANESE PATIENTS
    European journal of pediatrics
    
    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
15. VANDERBURGT I; BERENDS E; LOMMEN E; VANBEERSUM S; HAMEL B; MARIMAN E
    CLINICAL AND MOLECULAR STUDIES IN A LARGE DUTCH FAMILY WITH NOONAN SYNDROME
    American journal of medical genetics
    
    I. Vanderburgt et al., "CLINICAL AND MOLECULAR STUDIES IN A LARGE DUTCH FAMILY WITH NOONAN SYNDROME", American journal of medical genetics, 53(2), 1994, pp. 187-191
16. WEEMAES C; SMEETS D; BAKKEREN J; VANDERBURGT I
    ICF SYNDROME
    Pediatric research
    
    C. Weemaes et al., "ICF SYNDROME", Pediatric research, 36(1), 1994, pp. 10000065-10000065
17. SMEETS D; HAMERS A; VANDERBURGT I; ELSEVIER D; VANGAAL J; MERKX G; NIEHOFF J; VAESPEETERS G; WIENEN I; WEEMAES C
    ICF SYNDROME STUDIED BY FLUORESCENCE IN-SITU HYBRIDIZATION
    American journal of human genetics
    
    D. Smeets et al., "ICF SYNDROME STUDIED BY FLUORESCENCE IN-SITU HYBRIDIZATION", American journal of human genetics, 53(3), 1993, pp. 220-220