Showing results (141-150 of 1,050) with videos related to
Sort By:
Pageof 105
Tijdschrift Voor Kindergeneeskunde|April 1, 1992
[Pulmonary artery loop: a cause of life-threatening stridor in the young infant]J De Koster, H Devlieger, F De Zegher, et al.Annales De Genetique|January 1, 1987
Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedemaJ P Fryns, A Kleczkowska, P Moerman, et al.Annales De Genetique|January 1, 1987
The Roberts tetraphocomelia syndrome: identical limb defects in two siblingsJ P Fryns, A Kleczkowska, P Moerman, et al.Clinical Genetics|September 1, 1987
Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein?P Petit, M Bossens, D Thomas, et al.Bulletin De La Societe Belge D'Ophtalmologie|June 6, 2003
Incidence, perinatal risk factors, visual outcome and management of threshold retinopathyK Allegaert, N Verdonck, C Vanhole, et al.Pediatric Research|July 1, 1997
L-thyroxine treatment of preterm newborns: clinical and endocrine effectsC Vanhole, P Aerssens, G Naulaers, et al.Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.Human Genetics|November 1, 1989
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosomeJ Zhang, P Marynen, K Devriendt, et al.Prenatal Diagnosis|October 15, 2013
Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic herniaP D Brady, P DeKoninck, J P Fryns, et al.Pageof 105