Cognition genes on autosomes : the paradoxWILLEMS, P. J.Clinical genetics. 2007, Vol 72, Num 1, pp 9-12, issn 0009-9163, 4 p.Article

Genetic causes of hearing lossWILLEMS, P. J.The New England journal of medicine. 2000, Vol 342, Num 15, pp 1101-1109, issn 0028-4793Article

De invloed van omgevingsfactoren op verrichtingsgedrag: een kritiek op gangbare opvattingen en een voorstel tot heroriëntatie = L'influence de facteurs environmentaux sur la performance: critique de notions courantes et proposition d'une réorientation = Influence of environmental factors on performance: a critique of current notions and a proposal for a different approachWILLEMS, P. J.Nederlands tijddschrift voor de psychologie en haar grensgebieden. 1984, Vol 39, Num 2, pp 73-87, issn 0028-2235Article

PCR detection of a BclI RFLP in the G6PD gene of CaucasiansWILLEMS, P. J; VITS, L.Human genetics. 1992, Vol 89, Num 5, issn 0340-6717, p. 579Article

Bg/II RFLP in DXS 498 between the pigment gene repeat unit, RCP and GCPVITS, L; WILLEMS, P. J.Human genetics. 1992, Vol 90, Num 3, issn 0340-6717, p. 322Article

Genetic deficiencies of the glycogen phosphorylase systemHENDRICKX, J; WILLEMS, P. J.Human genetics. 1996, Vol 97, Num 5, pp 551-556, issn 0340-6717Article

Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13COUCKE, P. J; WESSELS, M. W; VAN ACKER, P et al.Journal of medical genetics. 2003, Vol 40, Num 10, pp 747-751, issn 0022-2593, 5 p.Article

Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472ENSINK, R. J. H; VERHOEVEN, K; MARRES, H. A. M et al.Archives of otolaryngology, head & neck surgery. 1998, Vol 124, Num 8, pp 886-891, issn 0886-4470Article

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pVAN CAMP, G; COUCKE, P. J; KENYON, J et al.Genomics (San Diego, Calif.). 1997, Vol 41, Num 1, pp 70-74, issn 0888-7543Article

Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15VAN LAER, L; VAN CAMP, G; GREEN, E. D et al.Human genetics. 1997, Vol 99, Num 6, pp 831-833, issn 0340-6717Article

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm of chromosome 11BARTSCH, O; WIM WUYTS; SHAFFER, L. G et al.American journal of human genetics. 1996, Vol 58, Num 4, pp 734-742, issn 0002-9297Article

X-linked liver glycogenosis type II (XLG II) is caused by mutations in PHKA2, the gene encoding the liver α subunit of phosphorylase kinaseHENDRICKX, J; DAMS, E; COUCKE, P et al.Human molecular genetics (Print). 1996, Vol 5, Num 5, pp 649-652, issn 0964-6906Article

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11YUAN-QING WU; HEUTINK, P; DE VRIES, B. B. A et al.Human molecular genetics (Print). 1994, Vol 3, Num 1, pp 167-171, issn 0964-6906Article

Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyCOUCKE, P; VITS, L; VAN CAMP, G et al.Human molecular genetics (Print). 1994, Vol 3, Num 4, pp 671-673, issn 0964-6906Article

On an autosomal dominant form of retinal-cerebellar degeneration : an autopsy study of five patients in one familyMARTIN, J.-J; VAN REGEMORTER, N; HAYEZ-DELATTE, F et al.Acta neuropathologica. 1994, Vol 88, Num 4, pp 277-286, issn 0001-6322Article

Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type I syndromeBECKERS, A; ABS, R; REYNIERS, E et al.The Journal of clinical endocrinology and metabolism. 1994, Vol 79, Num 5, pp 1498-1502, issn 0021-972XArticle

X-linked liver glycogenosis: localization and isolation of a candidate geneHENDRICKX, J; COUCKE, P; VAN DEN BERGH, I et al.Human molecular genetics (Print). 1993, Vol 2, Num 5, pp 583-589, issn 0964-6906Article

DXS89 (pTAK10) detects a homologous sequence on the Y chromosomeHENDRICKX, J; VITS, L; WILLEMS, P. J et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 2, pp 554-555, issn 0888-7543Article

Aldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1) : loss of heterozygosity for polymorphic chromosome 11 deoxyribonucleic acid markers, including the MEN1 locusBECKERS, A; ABS, R; WILLEMS, P. J et al.The Journal of clinical endocrinology and metabolism. 1992, Vol 75, Num 2, pp 564-570, issn 0021-972XArticle

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring : characterization by fluorescence in situ hybridization and DNA analysisMANGELSCHOTS, K; VAN ROY, B; CEULEMANS, B et al.Human genetics. 1992, Vol 89, Num 4, pp 407-413, issn 0340-6717Article

Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31→q32COUCKE, P; MANGELSCHOTS, K; SPELEMAN, F et al.Cytogenetics and cell genetics. 1991, Vol 57, Num 2-3, pp 120-122, issn 0301-0171Article

Two brothers with mental retardation discordant for the fragile-× syndromeVAN ROY, B. C; WILLEMS, P. J; VITS, L. J et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 122-125, issn 0148-7299, 4 p.Article

Picture of the monthWILLEMS, P. J; GERRITSEN, J; MULDER, H. J et al.American journal of diseases of children (1960). 1986, Vol 140, Num 1, pp 57-58, issn 0002-922XArticle

Genetic factors in non-syndromic congenital heart malformationsWESSELS, M. W; WILLEMS, P. J.Clinical genetics. 2010, Vol 78, Num 2, pp 103-123, issn 0009-9163, 21 p.Article

Non-syndromic, autosomal-recessive deafnessPETERSEN, M. B; WILLEMS, P. J.Clinical genetics. 2006, Vol 69, Num 5, pp 371-392, issn 0009-9163, 22 p.Article