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kw.\*:("DELETION BRAS COURT")

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DELETION OF THE SHORT ARM OF CHROMOSOME #9 (46, 9P-): A NEW DELETION SYNDROMEALFI O; DONNELL GN; CRANDALL BF et al.1973; SEM. HOP., ANN. GENET.; FR.; DA. 1973; VOL. 16; NO 1; PP. 17-22; ABS. FR.; BIBL. 19REF.Serial Issue

A CASE OF THE 18P-SYNDROMESUBRT I; BERANKOVA J.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 16; NO 4; PP. 359-360Serial Issue

A SHORT, RETARDED CHILD WITH A DELETION OF THE SHORT ARM OF CHROMOSOME 18(18P-) = UNE ENFANT HYPOTROPHIQUE, RETARDEE, AVEC UNE DELETION DU BRAS COURT DU CHROMOSOME 18(18P-)PARKER CE; DONNELL GN; MAVALWALA J et al.1973; CLIN. PEDIATR.; U.S.A.; DA. 1973; VOL. 12; NO 1; PP. 42-46; BIBL. 23REF.Serial Issue

DELETION OF SHORT ARM OF CHROMOSOME 18 WITH NORMAL LEVELS OF IGA = DELETION DU BRAS COURT DU CHROMOSOME 18 AVEC DES TAUX NORMAUX D'IGASABATER J; ANTICH J; LLUCH M et al.1972; J. MENTAL DEFIC. RES.; G.B.; DA. 1972; VOL. 16; NO 2; PP. 103-111; BIBL. 1 P.Serial Issue

18P-SYNDROMET. DELETION AF DEN KORTE ARM AF KROMOSOM NR. 18 = SYNDROME 18P-. DELETION DU BRAS COURT DU CHROMOSOME 181973; UGESKR. LAEGER; DANM.; DA. 1973; VOL. 135; NO 1; PP. 17; BIBL. 5REF.Serial Issue

PARTIELLE DELETION DES KURZEN ARMES EINES CHROMOSOMES 4 (WOLF-SYNDROM). ZWEI NEUE FAELLE = DELETION PARTIELLE DU BRAS COURT D'UN CHROMOSOME 4 (SYNDROME DE WOLF). DEUX NOUVEAUX CASSCHINZEL A; SCHMID W.1972; ARCH. GENET.; SCHWEIZ; DA. 1972; VOL. 45; NO 2; PP. 88-98; ABS. ANGL.; BIBL. 19REF.Serial Issue

FURTHER OBSERVATIONS ON A PREVIOUSLY REPORTED CASE OF 4P- SYNDROME = NOUVELLES OBSERVATIONS SUR UN CAS DEJA PUBLIE DE SYNDROME 4P-SUBRT I; BLEHOVA B.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 15; NO 4; PP. 361-363; BIBL. 4REF.Serial Issue

RING-CHROMOSOM 18. EIN 18P-/18Q-DELETIONSSYNDROM = CHROMOSOME 18 EN ANNEAU. UN SYNDROME DE DELETION 18P-/18Q-KUNZE J; STEPHAN E; TOLKSDORF M et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 15; NO 4; PP. 289-318; ABS. ANGL.; BIBL. 6P.Serial Issue

LE SYNDROME 18P-SERVILLE F; BATTIN J.1973; REV. INTERNATION. PEDIATR.; FR.; DA. 1973; NO 33; PP. 9-19 (9P.); BIBL. 1P.1/2Serial Issue

RHEUMATOID ARTHRITIS IN THE 46, XX, 18P-SYNDROME = ARTHRITE RHUMATOIDE DANS LE SYNDROME 46, XX, 18P-FINLEY SC; FINLEY WH; JOHNSON JC et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 6; PP. 465-469; BIBL. 23REF.Serial Issue

THE DENSITOMETRIC STUDY OF G BANDS ON HUMAN METAPHASE CHROMOSOMES = L'ETUDE DENSIMETRIQUE DES BANDESG SUR LES CHROMOSOMES HUMAINS EN METAPHASERADOVAN CHRZ; KOZAK J; MALKOVA J et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 2; PP. 149-154; ABS. ALLEM.; BIBL. 5REF.Serial Issue

MALFORMAZIONI SCHELETRICHE DA ABERRAZIONI CROMOSOMICHE = LES MALFORMATIONS SQUELETTIQUES DANS LES ABERRATIONS CHROMOSOMIQUESDALLAPICCOLA B; PISTOCCHI GF.1972; MINERVA MED.; ITAL.; DA. 1972; VOL. 63; NO 92; PP. 5049-5268; ABS. ANGL.; BIBL. 15REF.Serial Issue

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