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THE WOLF-HIRSCHHORN (4P-) SYNDROME.JOHNSON VP; MULDER RD; HOSEN R et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 104-112; BIBL. 2 P.Article

TWO CHILDREN WITH DELETION OF THE LONG ARM OF CHROMOSOME 4 WITH BREAKPOINT AT BAND Q33TOMKINS DJ; HUNTER AGW; UCHIDA IA et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 6; PP. 348-355; BIBL. 14 REF.Article

LETTER TO THE EDITOR: DELETION OF CHROMOSOME 4Q33->QTER. IS IT DIFFERENT FROM 4Q31->QTER DELETION SYNDROME.TUCHMAN M; EBRAHIMI J; GORLIN RJ et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 391-393; BIBL. 11 REF.Article

THE DEL(4)(Q31) SYNDROME: A RECOGNIZABLE DISORDER WITH ATYPICAL ROBIN MALFORMATION SEQUENCEDAVIS JM; CLARREN SK; SALK DJ et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 113-117; BIBL. 11 REF.Article

NEUROPATHOLOGICAL FINDINGS IN WOLF-HIRSCHHORN (4P-) SYNDROMEGOTTFRIED M; LAVINE L; ROESSMANN U et al.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 55; NO 2; PP. 163-165; BIBL. 15 REF.Article

BRIEF CLINICAL REPORT: PATHOLOGIC FINDINGS IN THE WOLF-HIRSCHHORN (4 P-) SYNDROMEGONZALEZ CH; CAPELOZZI VL; WAJNTAL A et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 183-187; BIBL. 5 REF.Article

NEUROLOGICAL AND NEUROPATHOLOGICAL FINDINGS IN RING CHROMOSOME 4YOUNG RSK; ZALNERAITIS EL.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 487-490; BIBL. 9 REF.Article

MONOSOME HQ 32.1->HQTER SURVENUE DE NOVO CHEZ UN NOUVEAU-NE MULTIMALFORMERETHORE MO; COUTURIER J; MSELATI JC et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 214-216; ABS. ENG; BIBL. 10 REF.Article

ANNEAU DU CHROMOSOME 4. II. SANS DYSMORPHIE FACIALE.CHAVIN COLIN F; TURLEAU C; LIMAL JM et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 105-109; ABS. ANGL.; BIBL. 12 REF.Article

TRISOMIE 4P DE NOVO PAR ISOCHROMOSOME 4P.ANDRE MJ; AURIAS A; DE BERRANGER P et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 2; PP. 127-131; ABS. ANGL.; BIBL. 16 REF.Article

POLYMORPHISM IN CHROMOSOME 4BARDHAN S; SINGH DN; DAVIS K et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 20; NO 1; PP. 44-47; BIBL. 13 REF.Article

THE 4P-SYNDROME IN A 24-YEAR-OLD FEMALEFRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 2; PP. 110-111; ABS. FRE; BIBL. 5 REF.Article

THE WOLF-HIRSCHHORN SYNDROME. DELETION OF THE SHORT ARM OF CHROMOSOME 4FRYNS JP; FRANCOIS B; TIMMERMANS J et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 2; PP. 135-139; BIBL. 12 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 4 FROM A SUBJECT WITH WOLF'S SYNDROME. REPOSITORY IDENTIFICATION NO.6M-72.BREG WR; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 5; PP. 307-308; BIBL. 5 REF.Article

RING CHROMOSOME 4 AND WOLF SYNDROME.PEREZ CASTILLO A; ABRISQUETA JA.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 1; PP. 87-91; BIBL. 9 REF.Article

A (2;4) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-1064.BIEDERMAN B; BOWEN P; ARONSON MM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 5; PP. 300-301; BIBL. 1 REF.Article

TERMINAL DELETION (4) (Q33) IN A MALE INFANTSTAMBERG J; WANG JABS E; ELIAS E et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 2; PP. 125-129; BIBL. 6 REF.Article

PARTIAL MONOSOMY OF LONG ARM OF CHROMOSOME 4 DUE TO INTERSTITIAL DELECTIONMCDERMOTT A; CAIN R; HOWELL R et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 3; PP. 305-307; BIBL. 8 REF.Article

DE NOVO TRISOMY 4PTER->Q21.HERVA R; VON WENDT L.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 2; PP. 225-230; BIBL. 16 REF.Article

PROXIMAL 4P-DELETION: PHENOTYPE DIFFERS FROM CLASSICAL 4P-SYNDROME.FRANCKE U; ARIAS DE; NYHAN WL et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 90; NO 2; PP. 250-252; BIBL. 6 REF.Article

LETTER TO THE EDITOR: DEL(4) (Q 31) SYNDROMECHUDLEY AE; PABELLO PD; BINGHAM W et al.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 341-343; BIBL. 2 REF.Article

BRIEF CYTOGENETIC CASE REPORT: A 4.5-YEAR-OLD GIRL WITH DELETION 4Q SYNDROME-DE NOVO, 46,XX,DEL(4) (PTER->Q31:)YOUNG RS; PALMER CG; BENDER HA et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 1; PP. 103-107; BIBL. 1 REF.Article

DELETIONS OF DIFFERENT SEGMENTS OF THE LONG ARM OF CHROMOSOME 4MITCHELL JA; PACKMAN S; LOUGHMAN WD et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 1; PP. 73-89; BIBL. 23 REF.Article

TERMINAL DELETION OF THE LONG ARM OF CHROMOSOME 4: REPORT OF A CASE OF 46,XY,DEL(4) (Q31) AND REVIEW OF 4Q-SYNDROMEYU CW; CHEN H; BAUCUM RW et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 158-161; ABS. FRE; BIBL. 12 REF.Article

THE WOLF-HIRSCHHORN SYNDROMELURIE IW; LAZJUK GI; LISSOVA YI et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 6; PP. 375-384; BIBL. 3 P.Article

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