Authors: LINDGREN AC HAGENAS L MULLER J BLICHFELDT S ROSENBORG M BRISMAR T RITZEN EM

Citation: Ac. Lindgren et al., GROWTH-HORMONE TREATMENT OF CHILDREN WITH PRADER-WILLI-SYNDROME AFFECTS LINEAR GROWTH AND BODY-COMPOSITION FAVORABLY, Acta paediatrica, 87(1), 1998, pp. 28-31

Authors: KJAER I WAGNER A MADSEN P BLICHFELDT S RASMUSSEN K RUSSELL B

Citation: I. Kjaer et al., THE SELLA TURCICA IN CHILDREN WITH LUMBOSACRAL MYELOMENINGOCELE, European journal of orthodontics (Print), 20(4), 1998, pp. 443-448

Authors: SCHULZE A HANSEN C BAEKGAARD P BLICHFELDT S PETERSEN MB TOMMERUP N BRONDUMNIELSEN K

Citation: A. Schulze et al., CLINICAL-FEATURES AND MOLECULAR-GENETIC ANALYSIS OF A BOY WITH PRADER-WILLI-SYNDROME CAUSED BY AN IMPRINTING DEFECT, Acta paediatrica, 86(8), 1997, pp. 906-910

Authors: LINDGREN AC HAGENAS L MULLER J BLICHFELDT S ROSENBORG M BRISMAR T RITZEN EM

Citation: Ac. Lindgren et al., EFFECTS OF GROWTH-HORMONE TREATMENT ON GROWTH AND BODY-COMPOSITION INPRADER-WILLI-SYNDROME - A PRELIMINARY-REPORT, Acta paediatrica, 86, 1997, pp. 60-62

Authors: SCHWARTZ M BLICHFELDT S MULLER J

Citation: M. Schwartz et al., X-LINKED ADRENAL HYPOPLASIA IN A LARGE GREENLANDIC FAMILY - DETECTIONOF A MISSENSE MUTATION (N440I) IN THE DAX-1 GENE - IMPLICATION FOR GENETIC-COUNSELING AND CARRIER DIAGNOSIS, Human genetics, 99(1), 1997, pp. 83-87

Authors: HAAGERUP A ANDERSEN JB BLICHFELDT S CHRISTENSEN MF

Citation: A. Haagerup et al., BIOTINIDASE DEFICIENCY - 2 CASES OF VERY EARLY PRESENTATION, Developmental Medicine and Child Neurology, 39(12), 1997, pp. 832-835