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

Une observation d'acrocéphalosyndactylie familiale = Report of a case of familial acrocephalosyndactylyLE MERRER, M; MAROTEAUX, P; FREZAL, J et al.Annales de pédiatrie (Paris). 1983, Vol 30, Num 9, pp 695-697, issn 0066-2097Article

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

Apparent Apert syndrome with polydactyly: rare pleiotropic manifestation or new syndrome?MAROTEAUX, P; FONFRIA, M. C.American journal of medical genetics. 1987, Vol 28, Num 1, pp 153-158, issn 0148-7299Article

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

A family with the Saethre-Chotzen syndromeBIANCHI, E; ARICO, M; PODESTA, A. F et al.American journal of medical genetics. 1985, Vol 22, Num 4, pp 649-658, issn 0148-7299Article

Apert syndrome and fetal hydrocephalyHYON KIM; VIJAY UPPAL; WALLACH, R et al.Human genetics. 1986, Vol 73, Num 1, pp 93-95, issn 0340-6717Conference Paper

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

ACROCEPHALOSYNDACTYLY = ACROCEPHALOSYNDACTYLIEGUPTA JL; PILLAI RR.1972; INTERNATION. SURG.; U.S.A.; DA. 1972; VOL. 57; NO 8; PP. 671-674; ABS. PORT. ESP. ALLEM. FR.; BIBL. 10 REF.Serial Issue

ZUR PATHOGENESE DER DYSKRANIE = SUR LA PATHOGENIE DE LA DYSCRANIESCHOENENBERG H.1972; KLIN. PEDIATR.; DTSCH.; DA. 1972; VOL. 184; NO 3; PP. 175-182; ABS. ANGL.; BIBL. 1 P.Serial Issue

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

THE SUMMITT SYNDROME: OBSERVATIONS ON A THIRD CASESELLS CJ; HANSON JW; HALL JG et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 1; PP. 27-33; BIBL. 3 REF.Article

FAMILIAL ACROCEPHALOSYNDACTYLY (PFEIFFER SYNDROME) = ACROCEPHALOSYNDACTYLIE FAMILIALE (SYNDROME DE PFEIFFER)SALDINO RM; STEINBACH HL; EPSTEIN CJ et al.1972; AMER. J. ROENTGENOL. RADIUM THERAPY NUCL. MED.; U.S.A.; DA. 1972; VOL. 116; NO 3; PP. 609-622; BIBL. 1P.1/2Serial Issue

AUTOSOMAL RECESSIVE ACROCEPHALOSYNDACTYLY REVISITEDHALL JG; REED SD; SELLS CJ et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 4; PP. 423-424; BIBL. 5 REF.Article

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