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L'ENCEPHALOPATHIE LIEE A LA FRAGILITE DU CHROMOSOME XMATTEI JF.1982; ARCHIVES FRANCAISES DE PEDIATRIE; ISSN 0003-9764; FRA; DA. 1982; VOL. 39; NO 8; PP. 633-639; BIBL. 81 REF.Article

FORMES INTEGRABLES HOLOMORPHES SINGULIERESCERVEAU D; MATTEI JF.1982; ASTERISQUE; ISSN 0303-1179; FRA; DA. 1982 PUBL. 1983; NO 97; 192 P.; BIBL. 53 REF.Serial Issue

RETARD MENTAL ET FRAGILITE DU CHROMOSOME X: FRA (X) (Q28)GIRAUD F; MATTEI JF.1981; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1981; VOL. 38; NO 5; PP. 387-388; BIBL. 19 REF.Article

HOLONOMIE ET INTEGRALES PREMIERESMATTEI JF; MOUSSU R.1980; ANN. SCI. EC. NORM. SUPER.; ISSN 0012-9593; USA; DA. 1980; VOL. 13; NO 4; PP. 469-523; BIBL. 25 REF.Article

L'ACIDE FOLIQUEVIDAL I; ROUX F; MATTEI JF et al.1982; MED. INFANT.; ISSN 0025-6773; FRA; DA. 1982; VOL. 89; NO 4; PP. 463-477; 13 P.; BIBL. 60 REF.Article

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

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

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

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

LA MALADIE DE WILSON: ETUDE ANATOMOCLINIQUE DE SIX OBSERVATIONSCHAPOY P; PERRIMOND H; DOR AM et al.1979; SEM. HOP.; FRA; DA. 1979; VOL. 55; NO 9-10; PP. 458-464; ABS. ENG; BIBL. 18 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

DYSTROPHIE THORACIQUE ET NEPHROPATHIE.COMBES JC; PICON G; FIESCHI JB et al.1977; SEM. HOP., ANN. PEDIATR.; FR.; DA. 1977; VOL. 53; NO 9; PP. 203-207; ABS. ANGL. ESP.; BIBL. 15 REF.Article

ETUDE DE L'ACTIVITE ENZYMATIQUE INTRA-ERYTHROCYTAIRE DANS LA TRISOMIE 21.MATTEI JF; VOVAN L; AYME S et al.1977; PEDIATRIE; FR.; DA. 1977; VOL. 32; NO 3; PP. 219-229; BIBL. 2 P.Article

PSEUDO-HERMAPHRODISME MALE INTERNE APPARENT. GYNECOMASTIE. RECHERCHE CHIRURGICALE DES GONADES NEGATIVES. CARYOTYPE 46, XX. PRESENCE D'ANTIGENE H-Y.VAGUE J; GUIDON J; MATTEI JF et al.1977; ANN. ENDOCRINOL.; FR.; DA. 1977; VOL. 38; NO 6; PP. 395-396; ABS. ANGL.; BIBL. 5 REF.Article

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

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

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