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kw.\*:("Dyschondrosteosis")

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DIE DYSCHONDROSTEOSE LERI-WEILL = LA DYSCHONDROSTEOSE DE LERI-WEILLKOCH HL.1983; ROEFOE. FORTSCHRITTE AUF DEM GEBIETE DER ROENTGENSTRAHLEN UND DER NUKLEARMEDIZIN; ISSN 0340-1618; DEU; DA. 1983; VOL. 138; NO 5; PP. 603-606; BIBL. 15 REF.Article

A POSSIBLY NEW FORM OF FAMILIAL BONE DYSPLASIA RESEMBLING DYSCHONDROSTEOSISFASANELLI S; IANNACCONE G; BELLUSSI A et al.1983; PEDIATRIC RADIOLOGY; ISSN 0301-0449; DEU; DA. 1983; VOL. 13; NO 1; PP. 25-31; BIBL. 14 REF.Article

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

SHOX mutations in a family and a fetus with langer mesomelic dwarfismTHOMAS, N. Simon; MALONEY, Viv; BASS, Paul et al.American journal of medical genetics. 2004, Vol 128A, Num 2, pp 179-184, issn 0148-7299, 6 p.Article

LA SINDROME DI LERI-WEILL: DESCRIZIONE DI UN CASO CLINICO = LE SYNDROME DE LERI-WEILL. DESCRIPTION D'UN CAS CLINIQUESALTI R; GALLUZZI F; FRANGINI V et al.1980; MINERVA PEDIATR.; ITA; DA. 1980; VOL. 32; NO 10; PP. 703-710; ABS. ENG; BIBL. 28 REF.Article

CLINICAL VARIATION IN DYSCHONDROSTEOSIS: A REPORT ON 13 INDIVIDUALS IN 8 FAMILIESDAWE C; WYNNE DAVIES R; FULFORD GE et al.1982; J. BONE JT. SURG. BR. VOL.; ISSN 0301-620X; GBR; DA. 1982; VOL. 64; NO 3; PP. 377-381; BIBL. 17 REF.Article

Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short statureBENITO-SANZ, Sara; AZA-CARMONA, Miriam; RODRIGUEZ-ESTEVEZ, Amaya et al.European journal of human genetics. 2012, Vol 20, Num 1, pp 125-127, issn 1018-4813, 3 p.Article

Enhancer elements upstream of the SHOX gene are active in the developing limbDURAND, Claudia; BANGS, Fiona; SIGNOLET, Jason et al.European journal of human genetics. 2010, Vol 18, Num 5, pp 527-532, issn 1018-4813, 6 p.Article

Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in langer mesomelic dysplasia (LMD)CAMPOS-BARROS, Angel; BENITO-SANZ, Sara; ROSS, Judith L et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 9, pp 933-938, issn 1552-4825, 6 p.Article

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

MADELUNG'S DEFORMITY AND DISCHONDROSTEOSISGELBERMAN RH; BAUMAN T.1980; J. HAND SURG.; USA; DA. 1980; VOL. 5; NO 4; PP. 338-340; BIBL. 9 REF.Article

LANGER TYPE OF MESOMELIC DWARFISM AS THE POSSIBLE HOMOZYGOUS EXPRESSION OF DYSCHONDROSTEOSISFRYNS JP; VAN DEN BERGHE H.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 21-27; BIBL. 16 REF.Article

LA DYSCHONDROSTEOSE: ASPECTS RADIOLOGIQUES, GENETIQUES ET ORTHOPEDIQUESDELAGOUTTE JP; CHANSON L; POLO M et al.1979; ANN. MED. NANCY EST; FRA; DA. 1979-05; VOL. 18; PP. 665-668; ABS. ENG; BIBL. 29 REF.Article

Translocation (Y;22) resulting in the loss of SHOX and isolated short statureBORIE, C; LEGER, J; DUPUY, O et al.American journal of medical genetics. 2004, Vol 125A, Num 2, pp 186-190, issn 0148-7299, 5 p.Article

MESOMELER ZWERGWUCHS VOM TYP LANGER ALS HOMOZYGOTE FORM DER DYSCHONDROSTEOSE = LE NANISME MESOMELIQUE DE TYPE LANGER, UNE FORME HOMOZYGOTE DE LA DYSCHONDROSTEOSEKEMPERDICK H; MAJEWSKI F.1982; ROEFOE, FORTSCHR. GEB. ROENTGENSTR. NUKLEARMED.; ISSN 0340-1618; DEU; DA. 1982; VOL. 136; NO 5; PP. 583-587; BIBL. 12 REF.Article

MADELUNG'S DEFORMITY. A FOLLOW-UP STUDY OF 26 CASES AND A REVIEW OF THE LITERATURE.NIELSEN JB.1977; ACTA ORTHOP. SCAND.; DANEM.; DA. 1977; VOL. 48; NO 4; PP. 379-384; BIBL. 34 REF.Article

Microdeletion in the SHOX 3' region associated with skeletal phenotypes of langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and leri-weill dyschondrosteosis in her 46,XX mother : Implication for the SHOX enhancerFUKAMI, Maki; OKUYAMA, Torayuki; YAMAMORI, Shunji et al.American journal of medical genetics. 2005, Vol 137A, Num 1, pp 72-76, issn 0148-7299, 5 p.Article

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

RADIOLOGICAL CASE OF THE MONTHYOUNG LW.1978; AMER. J. DIS. CHILD; USA; DA. 1978; VOL. 132; NO 10; PP. 1037Article

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

SEX-INFLUENCED EXPRESSION OF MADELUNG'S DEFORMITY IN A FAMILY WITH DYSCHONDROSTEOSISLICHTENSTEIN JR; MURALI SUNDARAM; BURDGE R et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 1; PP. 41-43; BIBL. 4 REF.Article

PRESENTAZIONE DI UN CASO DI DISCONDROSTEOSI CON STENOSI CANALARE LOMBARE E DOLICOFALANGIA = PRESENTATION D'UN CAS DE DYSCHONDROSTEOSE AVEC STENOSE CANALAIRE LOMBAIRE ET DOLICHOPHALANGIELEONE G.1979; RADIOL. MED.; ITA; DA. 1979; VOL. 65; NO 12; PP. 905-912; ABS. ENG; BIBL. 25 REF.Article

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