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Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1993
Confirmation of clinical diagnosis in requests for prenatal prediction of SMA type IJ M Cobben, M de Visser, H Scheffer, et al.
Human Genetics|March 1, 1996
Validation of the determination of deltaF508 mutations of the cystic fibrosis gene in over 11 000 mouthwashesH G de Vries, J M Collèe, M H van Veldhuizen, et al.
Patient Education and Counseling|November 14, 1997
Genetic counseling for hereditary cancer: a pilot study on experiences of patients and family membersE M Bleiker, N K Aaronson, F H Menko, et al.
Human Genetics|September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populationsH G de Vries, M A van der Meulen, R Rozen, et al.
The European Respiratory Journal|November 1, 1996
The nonhospital costs of care of patients with CF in The Netherlands: results of a questionnaireM F Wildhagen, J B Verheij, J G Verzijl, et al.
Prenatal Diagnosis|February 17, 2001
Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF)L Henneman, I Bramsen, T A Van Os, et al.
American Journal of Obstetrics and Gynecology|March 3, 2001
Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsiaA M Lachmeijer, R Arngrímsson, E J Bastiaans, et al.
Human Nutrition. Clinical Nutrition|March 1, 1987
Comparison of the fatty acid composition of human milk from mothers in Tanzania, Curacao and SurinamF A Muskiet, N H Hutter, I A Martini, et al.
Genomics|July 1, 1994
Identification of key recombinants in multiplex SMA familiesG van der Steege, J M Cobben, C Brahe, et al.
Neuromuscular Disorders : NMD|July 1, 1993
Linkage and apparent heterogeneity in proximal spinal muscular atrophiesJ M Cobben, H Scheffer, M De Visser, et al.
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