BOREDOM AT SCHOOLROBINSON W. P.BRITISH (THE) JOURNAL OF EDUCATIONAL PSYCHOLOGY. 1975, Vol 45, Num 2, pp 141-152Article

THE DIALOGUE OF DEFICIT AND DIFFERENCE IN LANGUAGE PROFICIENCYROBINSON W. P.LINGUISTICS. AN INTERNATIONAL REVIEW. 1975, Num 151, pp 27-40Article

Children's Explanation of Communication Failure and Inadequacy of the Misunderstood MessageROBINSON E. J; ROBINSON W. P.Developmental Psychology. 1977, Vol 13, Num 2, pp 156-161Article

THE GRAMMAR OF WORKING AND MIDDLE CLASS CHILDREN USING ELICITED IMITATIONSJORDAN C. M; ROBINSON W. P.LANG. SPEECH. 1972, Vol 15, Num 2, pp 122-140Article

THE GRAMMAR OF WORKING AND MIDDLE CLASS CHILDREN USING ELICITED IMITATIONSJORDAN C. M; ROBINSON W. P.LANGUAGE AND SPEECH. 1972, Vol 15, Num 2, pp 122-140Article

The extent mechanism, and consequences of genetic variation, for recombination rateROBINSON, W. P.American journal of human genetics. 1996, Vol 59, Num 6, pp 1175-1183, issn 0002-9297Article

Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriageHIRSCHFELD, A. F; JIANG, R; ROBINSON, W. P et al.Human reproduction (Oxford. Print). 2007, Vol 22, Num 2, pp 440-443, issn 0268-1161, 4 p.Article

Prenatally detected trisomy 20 mosaicismROBINSON, W. P; MCGILLIVRAY, B; LEWIS, M. E. S et al.Prenatal diagnosis. 2005, Vol 25, Num 3, pp 239-244, issn 0197-3851, 6 p.Article

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomyKUCHINKA, B. D; BARRETT, I. J; MOYA, G et al.Prenatal diagnosis. 2001, Vol 21, Num 1, pp 36-39, issn 0197-3851Article

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell lineBRUYERE, H; RUPPS, R; KUCHINKA, B. D et al.American journal of medical genetics. 2000, Vol 94, Num 1, pp 35-41, issn 0148-7299Article

The mechanisms involved in formation of deletions and duplications of 15q11-q13ROBINSON, W. P; DUTLY, F; NICHOLLS, R. D et al.Journal of medical genetics. 1998, Vol 35, Num 2, pp 130-136, issn 0022-2593Article

Angelman syndrome due to paternal uniparental disomy of chromosome 15 : a milder phenotype ?BOTTANI, A; ROBINSON, W. P; DELOZIER-BLANCHET, C. D et al.American journal of medical genetics. 1994, Vol 51, Num 1, pp 35-40, issn 0148-7299Article

Single-sex teaching and achievement in science = Enseignement non-mixte et progrès en scienceROBINSON, W. P; GILLIBRAND, E.International journal of science education. 2004, Vol 26, Num 6, pp 659-675, issn 0950-0693, 17 p.Article

Homelessness and strategies of Identity maintenance : A participant observation studyFARRINGTON, A; ROBINSON, W. P.Journal of community & applied social psychology. 1999, Vol 9, Num 3, pp 175-194, issn 1052-9284Article

Academic Achievement and Self-Esteem in Secondary School : Muddles, Myths and RealityROBINSON, W. P.Education research and perspectives. 1990, Vol 17, Num 1, pp 3-21, issn 0311-2543Article

Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted regionROBINSON, W. P; LALANDE, M.Human molecular genetics (Print). 1995, Vol 4, Num 5, pp 801-806, issn 0964-6906Article

Academic achievement and self-concepts of Latvian adolescents in a changed social context = Résultats scolaires et auto-perceptions des adolescents lettoniens dans un environnement social en transformationROBINSON, W. P; BRESLAV, G.European journal of psychology of education. 1996, Vol 11, Num 4, pp 399-410, issn 0256-2928Article

Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variationPENAHERRERA, M. S; JIANG, R; AVILA, L et al.Human reproduction (Oxford. Print). 2012, Vol 27, Num 6, pp 1745-1753, issn 0268-1161, 9 p.Article

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersBOURQUE, D. K; PENAHERRERA, M. S; YUEN, Rkc et al.Clinical genetics. 2011, Vol 79, Num 2, pp 169-175, issn 0009-9163, 7 p.Article

Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not PreeclampsiaBOURQUE, D. K; AVILA, L; PENAHERRERA, M et al.Placenta (Eastbourne). 2010, Vol 31, Num 3, pp 197-202, issn 0143-4004, 6 p.Article

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5ROBINSON, W. P; SLEE, J; SMITH, N et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 15, pp 1752-1759, issn 1552-4825, 8 p.Article

Recurrent trisomy 21 : four cases in three generationsGAIR, J. L; ARBOUR, L; RUPPS, R et al.Clinical genetics. 2005, Vol 68, Num 5, pp 430-435, issn 0009-9163, 6 p.Article

Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case-control studySTEPHENSON, M. D; AWARTANI, K. A; ROBINSON, W. P et al.Human reproduction (Oxford. Print). 2002, Vol 17, Num 2, pp 446-451, issn 0268-1161Article

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placentaPENAHERRERA, M. S; BARRETT, I. J; BROWN, C. J et al.Clinical genetics. 2000, Vol 58, Num 6, pp 436-446, issn 0009-9163Article

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restrictionROBINSON, W. P; BARRETT, I. J; BERNARD, L et al.American journal of human genetics. 1997, Vol 60, Num 4, pp 917-927, issn 0002-9297Article