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De novo inversion 1, in amniotic, fluid cell culturesSTÜHRENBERG, M.Human genetics. 1983, Vol 64, Num 4, issn 0340-6717, 412Article

ARE 1Q+ CHROMOSOMES HARMLESS. = LES CHROMOSOMES 1Q+ SONT-ILS INOFFENSIFS.GARDNER RJM; MCCREANOR HR; PARSLOW MI et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 5; PP. 383-393; BIBL. 1P.1/2Article

A (132) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-257ALFI OS; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 154-155Article

ETUDE CYTOGENETIQUE D'UN CAS DE SYNDROME DE FANCONI AVEC INVERSION PERICENTRIQUE FAMILIALE.CRIPPA L; FERRIER S.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 1; PP. 7-16; ABS. ANGL. ALLEM.; BIBL. 13 REF.Article

A (1; 15) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-126PRESCOTT GH; MCCAW BK; TOLBY BE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 84-85; BIBL. 1REF.Article

GIEMSA BANDING OF CHROMOSOME 1 QH+ AND LINKAGE ANALYSIS = COLORATION EN BANDES PAR LE GIEMSA D'UN CHROMOSOME 1 QH+ ET ANALYSE DES LIAISONSHOWARD PN; STODDARD GR; GODDARD MW et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 1; PP. 44-48; BIBL. 21 REF.Article

AN (X; 1) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-97PUNNETT HH; KISTERMACHER ML; GREENE AE et al.1974; CYTOGENET. CELL GENET; SWITZ.; DA. 1974; VOL. 13; NO 4; PP. 406-407; BIBL. 1 REF.Article

Apparition de novo d'une trisomie 1q partielle en mosaïque par translocation 1;9GAGNON, J. A; RICHER, C.-L; LEMIEUX, N et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 33-37, issn 0003-3995Article

Chiasma-derived genetic lengths and recombination fractions: a reciprocal translocation 46,XY,t(1; 22)(q32; q13)PALMER, R. W; HULTEN, M. A.Annals of human genetics. 1983, Vol 47, Num 4, pp 299-310, issn 0003-4800Article

Duplication of part of chromosome 1q: clinical report and review of literatureMICHELS, V. V; BERSETH, C. L; ÓBRIEN, J. F et al.American journal of medical genetics. 1984, Vol 18, Num 1, pp 125-134, issn 0148-7299Article

A(1; 17) TRANSLOCATION PLUS TRISOMY 21, 47 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-201DE LA CHAPELLE A; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 82-83Article

A 1Q42 DELETION IN A VIETNAMESE INFANTNEU RL; AVILA DA; REDDINGTON JM et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 154-155; ABS. FRE; BIBL. 2 REF.Article

INTERSTITIAL DELETION 2Q31->Q33BUCHANAN PD; RHODES RL; STEVENSON CE JR et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 121-126; BIBL. 2 P.Article

BREAK POINTS IN CHROMOSOME #1 ABNORMALITIES OF 218 HUMAN NEOPLASMSBRITO BABAPULLE V; ATKIN NB.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 3; PP. 215-225; BIBL. 79 REF.Article

FY X : DUFFY-ALLEL ODER CHROMOSOMEN-ABNORMITAET. = FY X : ALLELE DU SYSTEME DUFFY OU ANOMALIE CHROMOSOMIQUE.STUERNER KH; LANGE RL.1975; ARZTL. LAB.; DTSCH.; DA. 1975; VOL. 21; NO 3; PP. 106-110; ABS. ANGL.; BIBL. 17 REF.Article

A new case of deletion 1q 42 syndromeTOLKENDORF, E; HINKEL, G. K; GABRIEL, A et al.Clinical genetics. 1989, Vol 35, Num 4, pp 289-292, issn 0009-9163, 4 p.Article

Interstitial deletion of chromosome 1 (q23-q25), Report of a caseSILENGO, M. C; DAVI, G. F; BIANCO, R et al.Clinical genetics. 1984, Vol 25, Num 6, pp 549-552, issn 0009-9163Article

Clinical consequences of deletion 1p35WENGER, S. L; STEELE, M. W; BECKER, D. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, issn 0022-2593, 263Article

Translocation (1;6) in acute lymphoblastic leukemiaWERNER-FAVRE, C; BECK, D; ENGEL, E et al.Cytogenetics and cell genetics. 1984, Vol 38, Num 2, issn 0301-0171, 158Article

Deletion of the distal long arm of chromosome 1: a definable syndromeJOHNSON, V. P; HECK, L. J; CARTER, G. A et al.American journal of medical genetics. 1985, Vol 22, Num 4, pp 685-694, issn 0148-7299Article

Familial hypogonadism with a balanced reciprocal 1; 12 translocationHANDELSMAN, D. J; SMITH, A.Journal of medical genetics. 1983, Vol 20, Num 6, issn 0022-2593, 478Article

MEIOTIC FINDINGS IN HUMAN RECIPROCAL 1:3 TRANSLOCATIONMICIC MD; MICIC SR.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 4; PP. 442-443; BIBL. 8 REF.Article

GENETIC ASPECTS PF STRUCTURAL CHROMOSOME VARIANT 1QH+KLECZKOWSKA A; KUBINEN E.1980; GENET POLON.; POL; DA. 1980; VOL. 21; NO 1; PP. 119-124; H.T. 3; ABS. POL/RUS; BIBL. 29 REF.Article

PARACENTRIC INVERSION IN THE SHORT ARM OF CHROMOSOME 1DEROOVER J; FRYNS JP; HAEGEMAN J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 117-121; BIBL. 6 REF.Article

DELETION IN THE LONG ARM OF CHROMOSOME 1 FROM A SUBJECT WITH MULTIPLE CONGENITAL ANOMALIES. REPOSITORY IDENTIFICATION NO. GM-2025SEKHON GS; HILLMAN RE; YU R et al.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 21; NO 3; PP. 176Article

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