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au.\*:("VAN HAGEN, J. M")

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A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathiesMAJAVA, Marja; HOORNAERT, Kristien P; PETERSEN, Michael B et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 3, pp 258-264, issn 1552-4825, 7 p.Article

Feasibility and outcomes of multiplex ligation-dependent probe amplification on buccal smears as a screening method for microdeletions and duplications among 300 adults with an intellectual disability of unknown aetiologyPEPPINK, D; DOUMA-KLOPPENBURG, D. D; DE ROOIJ-ASKES, E. S. P et al.JIDR. Journal of intellectual disability research (Print). 2008, Vol 52, pp 59-67, issn 0964-2633, 9 p., 1Article

Regional underreporting of associated congenital anomalies in cleft patients in the netherlandsVAN DER VEEN, F. J. C; VAN HAGEN, J. M; BERKHOF, J et al.The Cleft palate-craniofacial journal. 2006, Vol 43, Num 6, pp 710-714, issn 1055-6656, 5 p.Article

CHARGE syndrome : The phenotypic spectrum of mutations in the CHD7 geneJONGMANS, M. C. J; ADMIRAAL, R. J; GEURTS VAN KESSEL, A et al.Journal of medical genetics. 2006, Vol 43, Num 4, pp 306-314, issn 0022-2593, 9 p.Article

Increased prevalences of left-handedness and left-eye sighting dominance in individuals with williams-beuren syndromeVAN STRIEN, J. W; HASELEN, G. C. Lagers-Van; VAN HAGEN, J. M et al.Neuropsychology, development, and cognition. Section A, journal of clinical and experimental neuropsychology. 2005, Vol 27, Num 8, pp 967-976, issn 1380-3395, 10 p.Article

Clinical presentations of patients with polyol abnormalitiesHUCK, J. H. J; VERHOEVEN, N. M; VAN HAGEN, J. M et al.Neuropediatrics. 2004, Vol 35, Num 3, pp 167-173, issn 0174-304X, 7 p.Article

Kabuki syndrome in son and low grade mosaic 45,X/46,XX in motherVAN HAGEN, J. M; KWEE, M. L; MADAN, K et al.Genetic counseling. 1996, Vol 7, Num 3, pp 201-206, issn 1015-8146Article

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