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COFFIN-LOWRY SYNDROME IN SIBSMATTEI JF; LAFRAMBOISE R; ROUAULT F et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 3; PP. 315-319; BIBL. 11 REF.Article

LA SINDROME DI COFFIN-SIRIS. CONTRIBUTO CLINICO = LE SYNDROME DE COFFIN-SIRIS. CONTRIBUTION CLINIQUEGIOVANNUCCI UZIELLA ML; SEMINARA S; NICOTINA PA et al.1980; MINERVA PEDIATR.; ITA; DA. 1980; VOL. 32; NO 4; PP. 245-254; ABS. ENG; BIBL. 17 REF.Article

LE SYNDROME DE COFFIN SIRIS. ETUDE CRITIQUE DE LA LITTERATURE A PROPOS D'UN CASFOASSO MF; HERMIER M; DESCOS B et al.1983; PEDIATRIE; ISSN 0031-4021; FRA; DA. 1983; VOL. 38; NO 2; PP. 111-117; ABS. ENG; BIBL. 15 REF.Article

PARTIAL TRISOMY 9 WITH RESEMBLANCE TO COFFIN-SIRIS SYNDROME.KUSHNICK T; ADESSA GM.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 3; PP. 237-239; BIBL. 5 REF.Article

Is this the Coffin-Siris Syndrome or the BOD Syndrome?BRAUTBAR, Ariel; RAGSDALE, Judith; SHINAWI, Marwan et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 3, pp 559-562, issn 1552-4825, 4 p.Article

PICTURE OF THE MOUTHGELLIS SS; FEINGOLD M.1978; AMER. J. DIS. CHILD.; USA; DA. 1978; VOL. 132; NO 12; PP. 1213-1214Article

THE COFFIN SYNDROME.FRYNS JP; VINKEN L; VAN DEN BERGHE H et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 271-276; BIBL. 7 REF.Article

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patientMARQUES PEREIRA, Patricia; HERON, Delphine; HANAUER, André et al.Human genetics. 2007, Vol 122, Num 5, pp 541-543, issn 0340-6717, 3 p.Article

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndromeSANTEN, Gijs W. E; ATEN, Emmelien; WESSELS, Marja W et al.Nature genetics. 2012, Vol 44, Num 4, pp 379-380, issn 1061-4036, 2 p.Article

12;14 translocation in coffin siris syndromePATEL, Z. M; MULYE, V. R; RAGHAVAN, K et al.Indian pediatrics. 1987, Vol 24, Num 5, pp 435-438, issn 0019-6061Article

Upper gastrointestinal malformations in coffin-siris syndromeKELLERMAYER, Richard; KITAGAWA, Seiji; REDEL, Carol A et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 13, pp 1519-1521, issn 1552-4825, 3 p.Article

Premature thelarche in Coffin-Siris syndromeBRUNETTI-PIERRI, Nicola; ESPOSITO, Valentina; SALERNO, Mariacarolina et al.American journal of medical genetics. 2003, Vol 121A, Num 2, pp 174-176, issn 0148-7299, 3 p.Article

LE SYNDROME DE COFFIN-SIRIS: A PROPOS D'UN CASPERRON PERNET FRANCOISE.1980; ; FRA; LYON: ASSOCIATION CORPORATIVE ETUD. MED.; DA. 1980; 149; 77 P.: ILL.; 30 CM; BIBL. 52 REF.; TH.: MED./LYON 1/1980Thesis

SINDROME DE COFFIN-SIRIS. = SYNDROME DE COFFIN-SIRISBOSCH BANYERAS IM; SALCEDO S; RAMOS R et al.1978; REV. ESP. PEDIATR.; ESP; DA. 1978; VOL. 34; NO 201; PP. 255-260; ABS. ENG; BIBL. 5 REF.Article

The Coffin―Siris Syndrome: A Proposed Diagnostic Approach and Assessment of 15 Overlapping CasesSCHRIER, Samantha A; BODURTHA, Joann N; SHALEV, Stavit A et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 1865-1876, issn 1552-4825, 12 p.Article

Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters : nosology and genetics of the Coffin-Siris syndromRABE, P; HAVERSKAMP, F; EMONS, D et al.American journal of medical genetics. 1991, Vol 41, Num 3, pp 350-354, issn 0148-7299Article

The Coffin-Siris syndrome in two siblingsFRANCESCHINI, P; CIRILLO SILENGO, M; BIANCO, R et al.Pediatric radiology. 1986, Vol 16, Num 4, pp 330-333, issn 0301-0449Article

THE COFFIN-SIRIS SYNDROMESCHINZEL A.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 3; PP. 449-452; BIBL. 6 REF.Article

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndromeTSURUSAKI, Yoshinori; OKAMOTO, Nobuhiko; FUKUSHIMA, Yoshimitsu et al.Nature genetics. 2012, Vol 44, Num 4, pp 376-378, issn 1061-4036, 3 p.Article

The coffin-siris syndromeQAZI, Q. H; HECKMAN, L. S; MARKOUIZOS, D et al.Journal of medical genetics. 1990, Vol 27, Num 5, pp 333-336, issn 0022-2593Article

Coffin-Siris-Syndrom bei einem 5jährigen Mädchen = Coffin Siris syndrome chez une fillette de 5 ans = The Coffin Siris syndrome in a 5 years old girlMEINECKE, P; ENGELBRECHT, R; SCHAEFER, E et al.Monatsschrift für Kinderheilkunde. 1986, Vol 134N9, pp 692-695, issn 0026-9298Article

THE COFFIN-SIRIS SYNDROME: A REPORT OF FOUR CASES AND REVIEW OF THE LITERATURELUCAYA J; GARCIA CONESA JA; BOSCH BANYERAS JM et al.1981; PEDIATR. RADIOL.; ISSN 0301-0449; DEU; DA. 1981; VOL. 11; NO 1; PP. 35-38; BIBL. 20 REF.Article

THE COFFIN-SIRIS SYNDROME.TUNNESSEN WW JR; MCMILLAN JA; LEVIN MB et al.1978; AMER. J. DIS. CHILD.; U.S.A.; DA. 1978; VOL. 132; NO 4; PP. 393-395; BIBL. 5 REF.Article

THE COFFIN-LOWRY SYNDROME. A FACIO DIGITAL MENTAL RETARDATION SYNDROME. A CASE REPORT.MERCHANT RH.1976; INDIAN PEDIATR.; INDIA; DA. 1976; VOL. 13; NO 3; PP. 247-249; BIBL. 4 REF.Article

Cardiomyopathy in Coffin-Lowry syndromeFACHER, Jennifer J; REGIER, Elizabeth J; JACOBS, Gretta H et al.American journal of medical genetics. 2004, Vol 128A, Num 2, pp 176-178, issn 0148-7299, 3 p.Article

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