Mild expression of the Pfeiffer syndromeRASMUSSEN, S. A; FRIAS, J. L.Clinical genetics. 1988, Vol 33, Num 1, pp 5-10, issn 0009-9163Article

Picture of the monthFEINGOLD, M.American journal of diseases of children (1960). 1983, Vol 137, Num 12, pp 1191-1192, issn 0002-922XArticle

Early surgical intervention in Apert's syndactylyBAROT, L. R; CAPLAN, H. S; UPTON, J et al.Plastic and reconstructive surgery (1963). 1986, Vol 77, Num 2, pp 282-287, issn 0032-1052Article

Intellectual development in Apert's syndrome: a long term follow up of 29 patientsPATTON, M. A; GOODSHIP, J; HAYWARD, R et al.Journal of medical genetics. 1988, Vol 25, Num 3, pp 164-167, issn 0022-2593Article

ON THE CLASSIFICATION OF THE ACROCEPHALOSYNDACTYLY SYNDROMES.ESCOBAR V; BIXLER D.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 3; PP. 169-178; BIBL. 40 REF.Article

A STUDY OF PARENTAL AGE EFFECTS ON THE OCCURRENCE OF FRESH MUTATIONS FOR THE APERT SYNDROME = ETUDE DES EFFETS DE L'AGE PARENTAL SUR L'APPARITION DES MUTATIONS NOUVELLES DU SYNDROME D'APERTERICKSON JD; COHEN MM JR.1974; ANN. HUM. GENET.; G.B.; DA. 1974; VOL. 38; NO 1; PP. 89-96; BIBL. 25 REF.Article

Syndrome de Saethre-Chotzen: observation d'un cas familial à pénétrance progressive = Saethre-Chotzen syndrome: report of one caseLEOU, E; NEGRESCO, D; TZILICA, D et al.Médecine et hygiène. 1989, Vol 47, Num 1813, pp 3113-3118, issn 0025-6749, 6 p.Article

THE ACROCEPHALOSYNDACTYLY SYNDROMES: A METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS.ESCOBAR V; BIXLER D.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 4; PP. 295-305; BIBL. 1 P. 1/2Article

VARIABLE EXPRESSION IN PFEIFFER SYNDROMESANCHEZ JM; CIACCI DE NEGROTTI T.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 73-75; BIBL. 6 REF.Article

ACROCEPHALOSYNDACTYLY. REPORT OF A CASE, WITH REVIEW OF THE LITERATURE = L'ACROCEPHALOSYNDACTYLIE. LE RAPPORT D'UN CAS AVEC ANALYSE DE LA LITTERATURERUBIN MB; PIROZZI DJ; HEATON CL et al.1972; AMER. J. MED.; U.S.A.; DA. 1972; VOL. 53; NO 1; PP. 127-130; BIBL. 21 REF.Serial Issue

ARE THE ACROCEPHALOSYNDACTYLY SYNDROMES VARIABLE EXPRESSIONS OF A SINGLE GENE DEFECT.ESCOBAR V; BIXLER D.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 139-154; BIBL. 2 P. 1/2Article

Akrozephalosyndaktylie ― Vogt-Syndrom = Acrocéphalosyndactylie. Syndrome de Vogt = Acrocephalosyndactyly ― Vogt syndromeFEHLOW, P; WALTHER, F.Psychiatrie, Neurologie und medizinische Psychologie. 1985, Vol 37, Num 6, pp 323-329, issn 0033-2739Article

Chotzen-Saethre-Syndrom mit Oligophrenie und psychischer Fehlenwicklung = Saethre-Chotzen syndrome with oligophrenia and psychic maldevelopmentFEHLOW, P; WALTHER, F.Psychiatrie, Neurologie und medizinische Psychologie. 1990, Vol 42, Num 6, pp 364-368, issn 0033-2739, 5 p.Article

Congenital embryonal rhabdomyosarcoma of the hand and Apert's syndromeCOHEN, M; GHOSH, L; SCHAFER, M. E et al.The Journal of hand surgery (St. Louis, Mo.). 1987, Vol 12A, Num 4, pp 614-617, issn 0363-5023Article

Le syndrome de Saethre-Chötzen. Une étude à propos de 17 cas = The Saethre-Chötzen syndrome. Report on 17 casesFERRI, J; SEILER, C; PIOT, B et al.Revue de stomatologie et de chirurgie maxillo-faciale. 1993, Vol 94, Num 5, pp 290-299, issn 0035-1768Article

PITFALLS OF GENETIC COUNSELLING IN PFEIFFER'S SYNDROMEBARAITSER M; BOWEN BRAVERY M; SALDANA GARCIA P et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 250-256; BIBL. 8 REF.Article

LA SINDROME DI SAETHRE-CHOTZEN: CONTRIBUTO CLINICO = LE SYNDROME DE SAETHRE-CHOTZEN: CONTRIBUTION CLINIQUEGALLUZZI F; SALTI R; MARIANELLI L et al.1980; MINERVA PEDIATR.; ITA; DA. 1980; VOL. 32; NO 5; PP. 325-328; ABS. ENG; BIBL. 11 REF.Article

SYNDROME D'APERT. A PROPOS D'UNE OBSERVATION PERSONNELLECHARNAY BARCELO CHRISTINE.1979; ; FRA; DA. 1979; 134; 112 P.: ILL.; 30 CM; BIBL. 110 REF.; TH.: MED./DIJON/1979Thesis

ACROCEPHALOPOLYSYNDACTYLY TYPE IV: A NEW GENETIC SYNDROME IN 3 SIBSGOODMAN RM; STERNBERG M; SHEM TOV Y et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 3; PP. 209-214; BIBL. 8 REF.Article

DYSOSTOSEN. AKROCEPHALOSYNDAKTYLIEN, SEGMENTIERUNGSSTOERUNGEN DER WIRBELSAEULE, SEGMENTALE STOERUNGEN DER LANGEN ROEHRENKNOCHEN, ANGEBORENE VERBIEGUNG DER LANGEN ROEHRENKNOCHEN = DYSOSTOSE. ACROCEPHALOSYNDACTYLIES, TROUBLES DE LA SEGMENTATION RACHIDIENNE, TROUBLES SEGMENTAIRES DES OS LONGS, COURBURES CONGENITALES DES OS LONGSBRUNGER HJ; SCHUSTER W.1976; ORTHOPAEDE; DTSCH.; DA. 1976; VOL. 5; NO 2; PP. 68-74; BIBL. 11 REF.Article

Le syndrome d'Apert : à propos d'une observation = Apert's syndrome: a case reportDOUTETIEN, C; LALEYE, A; TCHABI, S et al.Journal français d'ophtalmologie. 2003, Vol 26, Num 7, pp 738-742, issn 0181-5512, 5 p.Article

Syndrome de Saethre-Chotzen et syndrome de Holt-Oram : implication de deux nouveaux gènes de développement, TWIST en TBX5 = Two new human development gens, TWIST and TBX5 involved in Saethre-Chotzen and in Holt-Gram syndromes, respectivelyGILGENKRANTZ, S.MS. Médecine sciences. 1997, Vol 13, Num 4, pp 576-580, issn 0767-0974Article

Acrocephalosyndactyly of Apert-Pfeiffer type and polydactylyLINDEMANN, C; MEINECKE, P; WOLFF, G et al.Dysmorphology and clinical genetics. 1992, Vol 6, Num 4, pp 184-190, issn 0893-6633Article

Acrocephalopolysyndactyly type II―Carpenter syndrome: clinical spectrum and an attempt at unification with goodman and summit syndromesCOHEN, D. M; GREEN, J. G; MILLER, J et al.American journal of medical genetics. 1987, Vol 28, Num 2, pp 311-324, issn 0148-7299Article

Rubrique iconographique dirigée par C. Fauré et J. Ph. Montagne: syndrome de Pfeiffer = Pfeiffer syndrome: radiological case reportLANTERI, M; BONIOLI, E; RUFFA, G et al.Archives françaises de pédiatrie. 1985, Vol 42, Num 8, pp 717-718, issn 0003-9764Article