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ETUDE CHROMOSOMIQUE CHEZ LES PARENTS D'ENFANTS TRISOMIQUES 21GIRAUD F; MATTEI JF; MATTEI MG et al.1975; LYON, MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 241-251; ABS. ANGL.; BIBL. 2P.Article

STRUCTURAL ANOMALIES OF THE X CHROMOSOME AND INACTIVATION CENTERMATTEI MG; MATTEI JF; VIDAL I et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 401-408; BIBL. 2 P.Article

TRISOMY 21 FOR THE REGION 21Q223: IDENTIFICATION BY HIGH-RESOLUTION R-BANDING PATTERNSMATTEI JF; MATTEI MG; BAETEMAN MA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 409-411; BIBL. 9 REF.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

PERICENTRIC INVERSION, INV (9) (P22 Q32), IN THE FATHER OF A CHILD WITH A DUPLICATION-DELETION OF CHROMOSOME 9 AND GENE DOSAGE EFFECT FOR ADENYLATE KINASE-1MATTEI JF; MATTEI MG; ARDISSONE JP et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 2; PP. 129-136; BIBL. 13 REF.Article

FOUR NEW CASES OF DICENTRIC Y CHROMOSOMES.GIRAUD F; MATTEI JF; LUCAS C et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 249-260; BIBL. 1 P. 1/2Article

CONSTITUTIONAL CHROMOSOMAL BREAKAGE.GIRAUD F; AYME S; MATTEI JF et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 2; PP. 125-136; BIBL. 1 P. 1/2Article

DELETION PARTIELLE DU BRAS COURT D'UN CHROMOSOME XGIRAUD F; HARTUNG M; MATTEI JF et al.1974; ARCH. FR. PEDIATR.; FR.; DA. 1974; VOL. 31; NO 7; PP. 717-724; ABS. ANGL.; BIBL. 1 P. 1/2Article

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

ASPECTS GENETIQUES DES SITES FRAGILES AUTOSOMIQUES: A PROPOS DE 40 CASGUICHAOUA M; MATTEI MG; MATTEI JF et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 183-197; ABS. ENG; BIBL. 75 REF.Article

PARTIAL INVERSION OF THE SECONDARY CONSTRICTION OF CHROMOSOME 9. DOES IT EXIST .MATTEI MG; MATTEI JF; GUICHAOUA M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 310-316; BIBL. 1 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

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

EXPRESSION IN LYMPHOCYTE AND FIBROBLAST CULTURE OF THE FRAGILE X CHROMOSOME: A NEW TECHNICAL APPROACHMATTEI MG; MATTEI JF; VIDAL I et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 2; PP. 166-169; BIBL. 17 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

ANEMIE SIDEROBLASTIQUE IDIOPATHIQUE ACQUISE. 3 CAS AVEC LE MEME CHROMOSOME MARQUEUR SUPPLEMENTAIRE (47, MAR +).DOR JF; MATTEI JF; MATTEI MG et al.1977; PATHOL. BIOL.; FR.; DA. 1977; VOL. 25; NO 2; PP. 89-93; ABS. ANGL.; BIBL. 30 REF.Article

LE SYNDROME DU CHROMOSOME 13 EN ANNEAUGIRAUD F; EMBERGER JM; PINSARD N et al.1975; PEDIATRIE; FR.; DA. 1975; VOL. 30; NO 4; PP. 339-349; BIBL. 1 P. 1/2Article

PETIT CHROMOSOME SUBMETACENTRIQUE SURNUMERAIRE ET SYNDROME DES YEUX DE CHATGIRAUD F; MATTEI JF; HARTUNG M et al.1975; SEM. HOP., ANN. PEDIATR.,; FR.; DA. 1975; VOL. 51; NO 21; PP. 449-452; ABS. ANGL. ESP. ALLEM.; BIBL. 17 REF.Article

CLINICAL, ENZYME, AND CYTOGENETIC INVESTIGATIONS IN THREE NEW CASES OF TRISOMY 8PMATTEI JF; MATTEI MG; ARDISSONE JP et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 3; PP. 315-321; BIBL. 12 REF.Article

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