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Human Genetics|January 1, 1997
X-linked adrenal hypoplasia in a large Greenlandic family. Detection of a missense mutation (N4401) in the DAX-1 gene; implication for genetic counselling and carrier diagnosisM Schwartz, S Blichfeldt, J MüllerUgeskrift for Laeger|January 2, 1989
[CT in children with epilepsy. The value of cerebral CT in children with epilepsy]N H Rasmussen, S Blichfeldt, G Z OstergaardInternational Journal of Circumpolar Health|March 2, 2005
Epilepsy among children in GreenlandS Blichfeldt, T Bille, I M Nielsen, et al.Developmental Medicine and Child Neurology|January 20, 1998
Biotinidase deficiency: two cases of very early presentationA Haagerup, J B Andersen, S Blichfeldt, et al.European Journal of Orthodontics|October 1, 1998
The sella turcica in children with lumbosacral myelomeningoceleI Kjaer, A Wagner, P Madsen, et al.Ugeskrift for Laeger|November 20, 1989
[Utilization of medical services for children in an area of Copenhagen]M Fischerman, F J Andersen, K Andersen, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2000
Growth hormone treatment of patients with Prader-Willi syndrome. Swedish Growth Hormone Advisory GroupE M Ritzén, A C Lindgren, L Hagenäs, et al.Ugeskrift for Laeger|March 13, 1995
[Prader-Willi syndrome--clinical picture and genetics]A H Schulze, M B Petersen, S S Blichfeldt, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 24, 1997
Effects of growth hormone treatment on growth and body composition in Prader-Willi syndrome: a preliminary report. The Swedish National Growth Hormone Advisory GroupA C Lindgren, L Hagenäs, J Müller, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1997
Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defectA Schulze, C Hansen, P Baekgaard, et al.Pageof 2