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Dépistage de la trisomie 21 : où en sommes-nous ?AYME, S.MEDECINE SCIENCES. 1996, Vol 12, Num 3, pp 393-397Article

FORMAL ANALYSIS OF DYSMORPHISM: OBJECTIVE METHODS OF SYNDROME DEFINITIONPREUS M; AYME S.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 1; PP. 1-16; BIBL. 2 P.Article

MATERNAL-AGE EFFECT IN ANEUPLOIDY: DOES ALTERED EMBRYONIC SELECTION PLAY A ROLE.AYME S; ABBY LIPPMAN HAND.1982; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 4; PP. 558-565; BIBL. 33 REF.Article

Santé publique et maladies génétiquesAYME, S; et al.Réadaptation (Paris). 1991, Num 384, pp 3-26, issn 0484-0305Article

Fetal death rates in mothers of children with trisomy 21 (Down syndrome)LIPPMAN, A; AYME, S.Annals of human genetics. 1984, Vol 48, Num 4, pp 303-312, issn 0003-4800Article

AUTOSOMAL DOMINANT DUPLICATION OF THE RENAL COLLECTING SYSTEM, HEARING LOSS, AND EXTERNAL EAR ANOMALIES: A NEW SYNDROME.FRASER FC; AYME S; HALAL F et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 3; PP. 473-478; BIBL. 9 REF.Article

A PROPOS DE L'AGE MATERNEL DANS LA TRISOMIE 21MATTEI JF; AYME S; MATTEI MG et al.1979; J. GENET. HUM.; CHE; DA. 1979; VOL. 27; NO 1; PP. 77-78; BIBL. 2 REF.Article

ABNORMAL CHILDHOOD PHENOTYPES ASSOCIATED WITH THE SAME BALANCED CHROMOSOME REARRANGEMENTS AS IN THE PARENTSAYME S; MATTEI MG; MATTEI JF et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 7-12; BIBL. 10 REF.Article

A DYNAMIC STUDY IN TWO NEW CASES OF X CHROMOSOME TRANSLOCATIONS.MATTEI MG; MATTEI JF; AYME S et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 251-257; BIBL. 11 REF.Article

DERMATOGLYPHICS IN PARENTS OF CHILDREN WITH TRISOMY 21: EVALUATION OF THEIR INTEREST IN GENETIC COUNSELLINGAYME S; MATTEI MG; MATTEI JF et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 1; PP. 78-84; BIBL. 18 REF.Article

ETUDE CHROMOSOMIQUE CHEZ LES PARENTS D'ENFANTS TRISOMIQUES 21. ASSOCIATIONS ENTRE CHROMOSOMES ACROCENTRIQUESMATTEI JF; MATTEI MG; AYME S et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 1; PP. 29-48; ABS. ANGL.; BIBL. 14REF.Article

Evaluation épidémiologique : le cas particulier du diagnostic prénatal = Epidemiologic evaluation: the example of prenatal diagnosisAYME, S; JULIAN, C.Revue d'épidémiologie et de santé publique. 1991, Vol 39, pp S65-S73, issn 0398-7620, SUP1Article

L'analyse des arrêts de production en fonderie sous pression = Analysis of pressure die casting production stoppagesHEMON, Y; AYME, S.Fonderie, Fondeur d'aujourd'hui. 1985, Num 44, pp 19-25, issn 0249-3136Article

The Marshall and Stickler syndromes: objective rejection of lumpingAYME, S; PREUS, M.Journal of medical genetics. 1984, Vol 21, Num 1, pp 34-38, issn 0022-2593Article

X-AUTOSOME TRANSLOCATIONS: CYTOGENETIC CHARACTERISTICS AND THEIR CONSEQUENCESMATTEI MG; MATTEI JF; AYME S et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 4; PP. 295-309; BIBL. 3 P.Article

VARIABILITE INTERINDIVIDUELLE DES ASSOCIATIONS ENTRE CHROMOSOMES ACROCENTRIQUESMATTEI MG; SOUIAH N; AYME S et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 2; PP. 181-189; ABS. ENG; BIBL. 29 REF.Article

A PROPOS DU DIAGNOSTIC PRENATAL DES MALFORMATIONS DU MEMBRE SUPERIEURMATTEI JF; CRISTOFARI J; GAMERRE M et al.1980; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1980; VOL. 28; NO 3; PP. 225-232; ABS. ENG; BIBL. 7 REF.Article

ANOMALIES CHROMOSOMIQUES: FACTEURS DE RISQUE ACTUELLEMENT CONNUSAYME S; MATTEI JF; MATTEI MG et al.1980; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1980; VOL. 28; NO 3; PP. 155-178; ABS. ENG; BIBL. 106 REF.Article

DISTRIBUTION OF SPONTANEOUS CHROMOSOME BREAKS IN MANMATTEI MG; AYME S; AURRAN Y et al.1979; CYTOGENET CELL GENET.; CHE; DA. 1979; VOL. 23; NO 1-2; PP. 95-102; BIBL. 2 P.Article

LES INVERSIONS PERICENTRIQUES: A PROPOS DE 47 OBSERVATIONSGIRAUD F; MATTEI JF; MATTEI MG et al.1979; J. GENET. HUM.; CHE; DA. 1979; VOL. 27; NO 2; PP. 109-122; ABS. ENG; BIBL. 27 REF.Article

LE RISQUE DE TRISOMIE 21 DANS LA DESCENDANCE EN CAS DE TRANSLOCATION MATERNELLE T (7; 21).GIRAUD F; MATTEI JF; MATTEI MG et al.1977; NOUV. PRESSE MED.; FR.; DA. 1977; VOL. 6; NO 14; PP. 1233; BIBL. 1 REF.Article

IMPORTANCE DE LA TRISOMIE 21 EN GENETIQUE MEDICALE. A PROPOS DE 312OBSERVATIONSGIRAUD F; MATTEI JF; AYME S et al.1975; MARSEILLE MED.; FR.; DA. 1975; VOL. 112; NO 2; PP. 71-75; ABS. ANGL.; BIBL. 4REF.Article

Le gêne, la génétique et le généticienAYME, S; JULIAN, C.Sciences sociales et santé. 1988, Vol 6, Num 3-4, pp 199-204, issn 0294-0337Article

GENTIC: A COMPUTERIZED MEDICAL GENETIC CASE RECORD SYSTEMAYME S; AURRAN Y; GOUVERNET J et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 1; PP. 43-51; BIBL. 1 P.Article

MATERNAL AGE AND ORIGIN OF NON-DISJUNCTION IN TRISOMY 21MATTEI JF; AYME S; MATTEI MG et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 368-372; BIBL. 30 REF.Article

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