Wrist pain in the Madelung's deformity of dyschondrosteosisFAGG, P. S.Journal of hand surgery. British volume. 1988, Vol 13, Num 1, pp 11-15, issn 0266-7681Article

Dysplasie mésomélique de Reinhardt-Pfeiffer ou dyschondrostéose ? La distinction est-elle fondée ? A propos d'une observation familiale avec variabilité d'expression = Reinhardt-Pfeiffer mesomelic dysplasia or dyschondrosteosis syndrome. Is the distinction well founded? Report of a family with variable disease expressionTOUTAIN, A; SIRINELLI, D; PAILLET, C et al.Annales de pédiatrie (Paris). 1991, Vol 38, Num 1, pp 37-45, issn 0066-2097Article

Pseudoautosomal linkage of Hodgkin diseaseHORWITZ, M; WIERNIK, P. H.American journal of human genetics. 1999, Vol 65, Num 5, pp 1413-1422, issn 0002-9297Article

Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosisSHEARS, D. J; VASSAL, H. J; GOODMAN, F. R et al.Nature genetics. 1998, Vol 19, Num 1, pp 70-73, issn 1061-4036Article

The regulation of growth plate cartilage turnoverORTH, M. W.Journal of dairy science. 1998, Vol 82, pp 183-189, issn 0022-0302, SUP2Conference Paper

A novel class of pseudoautosomal region 1 deletions downstream of SHOX is associated with léri-weill dyschondrosteosisBENITO-SANZ, Sara; THOMAS, N. Simon; HEATH, Karen E et al.American journal of human genetics. 2005, Vol 77, Num 4, pp 533-544, issn 0002-9297, 12 p.Article

Leri-Weill syndrome (Dyschondrosteosis): a family studyMOHAN, V; GUPTA, R. P; HELMI, K et al.Journal of hand surgery. British volume. 1988, Vol 13, Num 1, pp 16-18, issn 0266-7681Article

Increased cortical area and thickness in the distal radius in subjects with SHOX-gene mutationFREDERIKSEN, A. L; HANSEN, S; BRIXEN, K et al.Bone (New York, NY). 2014, Vol 69, pp 23-29, issn 8756-3282, 7 p.Article

Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancerBENITO-SANZ, Sara; LUIS ROYO, Jose; ELISE HEATH, Karen et al.Journal of medical genetics. 2012, Vol 49, Num 7, pp 442-450, issn 0022-2593, 9 p.Article

Metacarpophalangeal pattern profile analysis in Leri-Weill dyschondrosteosisLAURENCIKAS, E; SÖDERMAN, E; GRIGELIONIENE, G et al.Acta radiologica (1987). 2005, Vol 46, Num 2, pp 200-207, issn 0284-1851, 8 p.Article

Complete SHOX deficiency causes Langer mesomelic dysplasiaZINN, Andrew R; FANGLIN WEI; LING ZHANG et al.American journal of medical genetics. 2002, Vol 110, Num 2, pp 158-163, issn 0148-7299Article

Léri-Weill syndrome associated with a pseudodicentric X;Y translocation chromosome and skewed X-inactivation: Implications for genetic counsellingBARALLE, D; WILLATT, L. R; SHEARS, D. J et al.American journal of medical genetics. 2000, Vol 95, Num 4, pp 391-395, issn 0148-7299Article

Madelung deformity as a feature of the Leri-Layani-Weill syndrome or dyschondrosteosisSHARIF, K; SAINT-MARTIN, C; CLAPUYT, P et al.Journal belge de radiologie (1907). 1997, Vol 80, Num 6, pp 292-293, issn 0021-7646Article

Madelung deformity in skeletally immature patients : Morphologic assessment using radiography, CT, and MRICOOK, P. A; YU, J. S; WIAND, W et al.Journal of computer assisted tomography. 1996, Vol 20, Num 4, pp 505-511, issn 0363-8715Article

Weil disease : Importance of imaging findings for early diagnosisHENK, C. B; KRAMER, L; SCHODER, M et al.Journal of computer assisted tomography. 1996, Vol 20, Num 4, pp 609-612, issn 0363-8715Article

Dyschondrostéose de Léri-Weill associée à un adénome parathyroïdien sécrétant = Leri-Weill dyschondrosteosis syndrome with a functional parathyroid adenomaDONNET, A; QUINSAT, D; BOUCHACOURT, M et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 34, pp 2118-2119, issn 0037-1777Article

SHOX mutations in idiopathic short stature and leri-weill dyschondrosteosis : frequency and phenotypic variabilityJORGE, Alexander A. L; SOUZA, Silvia C; NISHI, Miriam Y et al.Clinical endocrinology (Oxford. Print). 2007, Vol 66, Num 1, pp 130-135, issn 0300-0664, 6 p.Article

Metacarpophalangeal pattern profile analysis : Useful diagnostic tool for differentiating between dyschondrosteosis, turner syndrome, and hypochondroplasiaLAURENCIKAS, E; SAVENDAHL, L; JORULF, H et al.Acta radiologica (1987). 2006, Vol 47, Num 5, pp 518-524, issn 0284-1851, 7 p.Article

Expression of SHOX in human fetal and childhood growth plateMUNNS, C. J. F; HAASE, H. R; CROWTHER, L. M et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 8, pp 4130-4135, issn 0021-972X, 6 p.Article

Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaROSS, Judith L; BELLUS, Gary; SCOTT, Charles I et al.American journal of medical genetics. 2003, Vol 116A, Num 1, pp 61-65, issn 0148-7299, 5 p.Article

Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosisVASSAL, Humberto; MEDEIRA, Ana; CORDEIRO, Isabel et al.American journal of medical genetics. 2001, Vol 99, Num 4, pp 331-334, issn 0148-7299Article

Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X maleSTUPPIA, L; CALABRESE, G; PALKA, G et al.Journal of medical genetics. 1999, Vol 36, Num 9, pp 711-713, issn 0022-2593Article

X/Y translocation in a family with Leri-Weill dyschondrosteosisCALABRESE, G; FISCHETTO, R; STUPPIA, L et al.Human genetics. 1999, Vol 105, Num 4, pp 367-368, issn 0340-6717Article

A SHOXing new kind of inheritanceClinical genetics. 1999, Vol 56, Num 4, pp 264-266, issn 0009-9163Article

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)BELIN, V; CUSIN, V; VIOT, G et al.Nature genetics. 1998, Vol 19, Num 1, pp 67-69, issn 1061-4036Article