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kw.\*:("DELETION C8 BRAS COURT")

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A NEW CHROMOSOME DELETION SYNDROME. REPORT OF A PATIENT WITH A 46, XY, 8 P-CHROMOSOME CONSTITUTIONORYE E; CRAEN M.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 3; PP. 289-301; BIBL. 17 REF.Article

CONTRIBUTION A L'ETUDE DES DELETIONS DU BRAS COURT DU CHROMOSOME 8. A PROPOS D'UNE OBSERVATION PERSONNELLE DEL (8) (P22->PTEI)THAO BOUNPRASEUTH.1979; ; FRA; DA. 1979; 838; 40 P.: ILL.; 30 CM; BIBL. 34 REF.; TH.: MED./LYON 1/1979Thesis

SMALL STRUCTURAL CHANGES OF CHROMOSOME 8. TWO CASES WITH EVIDENCE FOR DELETION.BEIGHLE C; KARP LE; HANSON JW et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 113-121; BIBL. 1 P. 1/2Article

A CASE OF DELETION OF SHORT ARM OF CHROMOSOME 8.LEISTI J; AULA P.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 187-194; BIBL. 4 REF.Article

DELETION PARTIELLE DU BRAS COURT DU CHROMOSOME 8TAILLEMITE JL; CHANNAROND J; TINEL H et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 251-255; ABS. ANGL.; BIBL. 15 REF.Article

DELETION PARTIELLE DU BRAS COURT DU CHROMOSOME 8.BRESSON JL; NOIR A; SCHERRER M et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 1; PP. 70-72; ABS. ANGL.; BIBL. 6 REF.Article

RDNA AND ACROCENTRIC CHROMOSOMES IN MAN. I. RDNA LEVELS IN A SUBJECT CARRIER OF A 8P/13P BALANCED TRANSLOCATION AND IN HIS UNBALANCED SON.GUANTI G; MOLLICA G; POLIMENO L et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 103-107; BIBL. 10 REF.Article

COMPUTER-ASSISTED ANALYSIS OF CHROMOSOMAL ABNORMALITIES: DETECTION OF A DELETION IN ANIRIDIA/WILMS'TUMOR SYNDROME = ANALYSE A L'AIDE D'ORDINATEUR D'ANOMALIES CHROMOSOMIQUES: DETECTION D'UNE DELETION DANS LE SYNDROME ANIRIDIE/TUMEURS DE WILMSLADDA R; ATKINS L; LITTLEFIELD J et al.1974; SCIENCE; U.S.A.; DA. 1974; VOL. 185; NO 4153; PP. 784-787; BIBL. 13REF.Article

THE 8P- SYNDROMEREISS JA; BRENES PM; CHAMBERLIN J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 135-140; BIBL. 14 REF.Article

NEW CHROMOSOMAL MALFORMATION SYNDROMES. I. PARTIAL MONOSOMY 8 P. AN ATTEMPT TO ESTABLISH A NEW CHROMOSOME DELETION SYNDROME.RODEWALD A; STENGEL RUTKOWSKI S; SCHULZ P et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 125; NO 1; PP. 45-57; ABS. ALLEM.; BIBL. 13 REF.Article

EXCLUSION DE MNSS, KIDD ET GM DE L'EXTREMITE DU BRAS COURT DU CHROMOSOME 8BIGGIO B; PHILIP T; CHARRIN C et al.1979; J. GENET. HUM.; CHE; DA. 1979; VOL. 27; NO 3; PP. 253-258; BIBL. 13 REF.Article

PARTIAL DUPLICATION 5Q SYNDROME: PHENOTYPIC SIMILARITY IN TWO SISTERS WITH IDENTICAL KARYOTYPE (PARTIAL DUPLICATION 5Q33->5QTER AND PARTIAL DEFICIENCY (8P23->PTER).BARTSCH SANDHOFF M; LIERSCH R.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 281-284; ABS. FR.; BIBL. 5 REF.Article

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