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Genetic heterogeneity among craniosynostosis syndromes : mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pLEWANDA, A. F; COHEN, M. M; HAUSELMAN, E et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 1, pp 115-119, issn 0888-7543Article

Saethre-Chotzen syndrome associated with balanced translocations involving 7p21 : three further familiesWILKIE, A. O. M; YANG, S. P; SUMMERS, D et al.Journal of medical genetics. 1995, Vol 32, Num 3, pp 174-180, issn 0022-2593Article

Renal tubular dysgenesis and very large cranial fontanels in a family with acrocephalosyndactyly S.C. typeRUSSO, R; D'ARMIENTO, M; VECCHIONE, R et al.American journal of medical genetics. 1991, Vol 39, Num 4, pp 482-485, issn 0148-7299, 4 p.Article

Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome ?PREIS, S; KAEWEL, E.-V; MAJEWSKI, F et al.Clinical genetics. 1995, Vol 47, Num 5, pp 267-269, issn 0009-9163Article

Saethre-Chotzen syndrome (ACS III) in four generationsNIEMANN-SEYDE, S. C; EBER, S. W; ZOLL, B et al.Clinical genetics. 1991, Vol 40, Num 4, pp 271-276, issn 0009-9163Article

Saethre-Chotzen Syndrome: A Case ReportPENA, William A; SLAVOTINEK, Anne; OBEROI, Snehlata et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 3, pp 318-321, issn 1055-6656, 4 p.Article

LES GÈNES TWIST : DE L'ÉTUDE DES SÉQUENCES RÉGULATRICES D'UN GÈNE DU DÉVELOPPEMENT EMBRYONNAIRE MURIN A L'INDENTIFICATION D'UN GÈNE IMPLIQUÉ DANS UN SYNDROME GÉNÉTIQUE HUMAIN = THETWIST GENES : FROM THE REGULATORY SEQUENCES ANALYSIS OF A MURINE EMBRYONIC DEVELOPMENTAL GENE TO THE IDENTIFICATION OF A GENE IMPLIED IN A HUMAN GENETIC SYNDROMEBourgeois, Patrice; Perrin Schmitt, Fabienne.1997, 206 p.Thesis

Possible genetic heterogeneity in the Saethre-Chotzen syndromeMA, H. W; LAJEUNIE, E; DE PARSEVAL, N et al.Human genetics. 1996, Vol 98, Num 2, pp 228-232, issn 0340-6717Article

Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patientLEWANDA, A. F; GREEN, E. D; CLARREN, S. K et al.American journal of human genetics. 1994, Vol 55, Num 6, pp 1195-1201, issn 0002-9297Article

The Frequency of Palatal Anomalies in Saethre-Chotzen SyndromeSTOLER, Joan M; ROGERS, Gary F; MULLIKEN, John B et al.The Cleft palate-craniofacial journal. 2009, Vol 46, Num 3, pp 280-284, issn 1055-6656, 5 p.Article

Saethre-Chotzen syndrome with trigonocephalyCRISTOFORI, G; FILIPPI, G.American journal of medical genetics. 1992, Vol 44, Num 5, pp 611-614, issn 0148-7299Article

Q289P mutation in FGFR2 gene causes saethre-chotzen syndrome : Some considerations about familial heterogeneityLOPES BURRONE DE FREITAS, Erika Cristina; DANTAS NASCIMENTO, Sandra Regina; PALANDI DE MELLO, Maricilda et al.The Cleft palate-craniofacial journal. 2006, Vol 43, Num 2, pp 142-147, issn 1055-6656, 6 p.Article

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutationsPAZNEKAS, W. A; CUNNINGHAM, M. L; MULLIKEN, J et al.American journal of human genetics. 1998, Vol 62, Num 6, pp 1370-1380, issn 0002-9297Article

Craniosynostosis suggestive of Saethre-Chotzen syndrome : Clinical description of a large kindred and exclusion of candidate regions on 7pVON GERNET, S; SCHUFFENHAUER, S; GOLLA, A et al.American journal of medical genetics. 1996, Vol 63, Num 1, pp 177-184, issn 0148-7299Article

Familial Saethre-Chotzen syndrome with or without polydactyly of the toeSHIDAYAMA, R; HIRANO, A; IIO, Y et al.Annals of plastic surgery. 1995, Vol 34, Num 4, pp 435-440, issn 0148-7043Article

Neuropsychiatrische Begleitsymptome bei Saethre-Chotzen-Syndrom = Saethre-Chotzen syndrome (SCS) and associated neurological and psychiatric symptomsFEHLOW, P; FRÖHLICH, B; MIOSGE, W et al.Fortschritte der Neurologie, Psychiatrie. 1992, Vol 60, Num 2, pp 66-73, issn 0720-4299Article

THE SAETHRE-CHOTZEN SYNDROME = LE SYNDROME DE SAETHRE-CHOTZENPANTKE OA; COHEN MM JR; WITKOP CJ JR et al.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 190-225; BIBL. 34 REF.Article

ROENTGENCEPHALOMETRIC STUDIES OF THE PREMATURE CRANIOFACIAL SYNOSTOSES: REPORT OF A FAMILY WITH THE SAETHRE-CHOTZEN SYNDROME. = ETUDES RADIOCEPHALOMETRIQUES DES SYNOSTOSES CRANIO-FACIALES PREMATUREES: OBSERVATION D'UNE FAMILLE AVEC SYNDROME DE SAETHRE-CHOTZENPRUZANSKY S; PASHAYAN H; KREIBORG S et al.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 226-237; BIBL. 12 REF.Article

Sindrome de Saethre-Chotzen. Estudio de una familia = Syndrome de Saethre Chotzen. Etude d'une famille = Saethre Chotzen syndrome. Study of a familyBORBOLLA, L; MENENDEZ, I; HERNANDEZ, M et al.Revista cubana de pediatría. 1984, Vol 56, Num 3, pp 359-370, issn 0034-7531Article

The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesROSE, C. S. P; PATEL, P; REARDON, W et al.Human molecular genetics (Print). 1997, Vol 6, Num 8, pp 1369-1373, issn 0964-6906Article

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndromeHOWARD, T. D; PAZNEKAS, W. A; GREEN, E. D et al.Nature genetics. 1997, Vol 15, Num 1, pp 36-41, issn 1061-4036Article

Evidence for locus heterogeneity in acrocephalosyndactyly : a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p-and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5qVAN HERWERDEN, L; ROSE, C. S. P; REARDON, W et al.American journal of human genetics. 1994, Vol 54, Num 4, pp 669-674, issn 0002-9297Article

Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22DOLLFUS, Helene; KUMARAMANICKAVEL, Govindasamy; BISWAS, Partha et al.Journal of medical genetics. 2001, Vol 38, Num 7, pp 470-471, issn 0022-2593Article

TWIST gene mutation in a patient with radial aplasia and craniosynostosis : Further evidence for heterogeneity of Baller-Gerold syndromeGRIPP, K. W; STOLLE, C. A; CELLE, L et al.American journal of medical genetics. 1999, Vol 82, Num 2, pp 170-176, issn 0148-7299Article

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22REID, C. S; MCMORROW, L. E; MCDONALD-MCGINN, D. M et al.American journal of medical genetics. 1993, Vol 47, Num 5, pp 637-639, issn 0148-7299Article

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