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kw.\*:("DELETION E18 BRAS LONG")

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UN CAS DE 18Q- AVEC ETUDE DU DEVELOPPEMENT PSYCHO-MOTEUR DE LA NAISSANCE A L'AGE DE 8 ANSGILGENKRANTZ S; RAVAILLE G; CABROL C et al.1974; REV. PEDIATR.; FR.; DA. 1974; VOL. 10; NO 8; PP. 507-514 (6 P.); ABS. ANGL.; BIBL. 30 REF.Article

BEITRAG ZUM BILD DES 18Q-SYNDROMS = COMMUNICATION SUR LA SYMPTOMATOLOGIE OBSERVEE DANS LE SYNDROME 18QFEICHTINGER C; GLATZL J.1974; WIEN. KLIN. WSCHR.; OESTERR.; DA. 1974; VOL. 86; NO 15; PP. 441-444; ABS. ANGL.; BIBL. 15REF.Article

PARTIAL TRISOMY 4Q AND PARTIAL MONOSOMY 18Q AS CONSEQUENCE OF A PATERNAL BALANCED TRANSLOCATION T(4Q; 18Q+)FONATSCH C; FLATZ SD; HURTER P et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 25; NO 3; PP. 227-233; BIBL. 8REF.Article

A CASE OF RING 18 CHROMOSOME IN A SIBSHIP WITH MULTIPLE SPONTANEOUS ABORTIONSCOCO R; BARREIRO CZ; PENCHASZADEH VB et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 135-137; ABS. FR.; BIBL. 3REF.Article

SYNDROMES ASSOCIATED WITH DELETION OF THE LONG ARM OF CHROMOSOME 18(DEL(18Q))WILSON MG; TOWNER JW; FORSMAN I et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 2; PP. 155-174; BIBL. 32 REF.Article

DUPLICATION-DEFICIENCY OF A CHROMOSOME 18, RESULTING FROM RECOMBINATION OF A PATERNAL PERICENTRIC INVERSION, WITH A NOTE FOR GENETIC COUNSELLINGTEYSSIER JR; BAJOLLE F.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 195-200; BIBL. 22 REF.Article

P-SYNDROME RESULTING FROM 14Q/18Q "DICENTRIC" FUSION TRANSLOCATION.FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 243-250; BIBL. 16 REF.Article

STRUCTURAL ABERRATIONS OF CHROMOSOME 18. II.THE 18Q-SYNDROME. REPORT OF THREE CASES = LES ABERRATIONS DE STRUCTURE DU CHROMOSOME 18. SYNDROME 18Q. OBSERVATION DE TROIS CASSCHINZEL A; HAYASHI K; SCHMID W et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 2; PP. 123-132; ABS. ALLEM.; BIBL. 2P.Article

Q-SYNDROME RESULTING FROM A T DIC (14P; 18Q)LAMBERT JC; FERRARI M; BERGONDI C et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 61-66; BIBL. 22 REF.Article

DISTAL 18Q DELETION WITHOUT CLINICAL FINDINGS OF 18Q-SYNDROMEQAZI QH; MADAHAR C; ALVI S et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 1; PP. 60-62; ABS. FRE; BIBL. 6 REF.Article

9-SYNDROME IN MOTHER AND DAUGHTERFRYNS JP; LOGGHE N; VAN EYGEN M et al.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 130; NO 3; PP. 189-192; BIBL. 6 REF.Article

TRANSLOCATION 46XY, T(17;18)(Q25;Q21) IN A MENTALLY RETARDED BOY WITH PROGRESSIVE EYE ABNORMALITIESSMITH A; CARADUS V; HENRY JG et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 156-162; BIBL. 13 REF.Article

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