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Results 1 to 25 of 31907

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FAMILIAL Y-AUTOSOME TRANSLOCATION IN TWO UNRELATED GIRLSFUNDERBURK SJ; KLISAK I; SPARKES RS et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 119-122; ABS. FRE; BIBL. 24 REF.Article

MEIOTIC AND SYNAPTONEMAL COMPLEX STUDIES IN A 14/21 TRANSLOCATION CARRIERVIDAL F; TEMPLADO C; NAVARRO J et al.1982; INT. J. ANDROL.; ISSN 0105-6263; DNK; DA. 1982; VOL. 5; NO 1; PP. 21-26; BIBL. 17 REF.Article

MODERATE DOWN'S SYNDROME IN THREE SIBLINGS HAVING PARTIAL TRISOMY 21Q22.2->QTER AND THEREFORE NO SOD-1 EXCESSHADEBANK M; RODEWALD A.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 74-77; BIBL. 12 REF.Article

VARIANT TRANSLOCATION IN A NON ENDEMIC CASE OF BURKITT'S LYMPHOMA: T(8;22) IN AN EPSTEIN-BARR VIRUS NEGATIVE TUMOUR AND IN A DERIVED CELL LINEBERTRAND S; BERGER R; PHILIP T et al.1981; EUR. J. CANCER; ISSN 0014-2964; GBR; DA. 1981; VOL. 17; NO 5; PP. 577-584; BIBL. 17 REF.Article

UN CAS DE TRISOMIE 22 INCOMPLETE DUE A LA MALSEGREGATION MEIOTIQUE D'UNE TRANSLOCATION FAMILIALE 11:22PESCIA G; JOTTERAND BELLOMO M; GAIDE AC et al.1981; REV. MED. SUISSE ROMANDE; ISSN 0035-3655; CHE; DA. 1981; VOL. 101; NO 4; PP. 325-329; BIBL. 6 REF.Article

COMPLEX CHROMOSOME REARRANGEMENTS. REPORT OF A NEW CASE AND LITERATURE REVIEWPAI GS; THOMAS GH; MAHONEY W et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 436-444; BIBL. 1 P.Article

TRISOMIE PARTIELLE 11Q PAR MALSEGREGATION D'UNE TRANSLOCATION MATERNELLE T(11; 22) (P23; P11.1)PANGALOS C; COUTURIER J; BARTSOCAS C et al.1980; NOUV. PRESSE MED.; ISSN 0301-1518; FRA; DA. 1980; VOL. 9; NO 41; PP. 3065-3067; ABS. ENG; BIBL. 7 REF.Article

OMPHALOCELE AND PARTIAL TRISOMY 1Q SYNDROMECHEN H; GERSHANIK JJ; MAILHES JB et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 1-4; BIBL. 27 REF.Article

TWO CHILDREN WITH PARTIAL TRISOMY FOR 7PBERRY AC; HONEYCOMBE J; MACOUN SJR et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 4; PP. 320-321; BIBL. 2 REF.Article

SINDROME 18P - DA TRASLOCAZIONE 18/21 = SYNDROME 18P - PAR TRANSLOCATION 18/21FERRANTE E; CHESSA L; BRUNI L et al.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 8; PP. 657-664; ABS. ENG; BIBL. 2 P.Article

PARTIAL TRISOMY 7P IN TWO FAMILIES RESULTING FROM DIFFERENT BALANCED TRANSLOCATIONSMOORE CM; PFEIFFER RA; CRAIG HOLMES AP et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 2; PP. 112-121; BIBL. 13 REF.Article

A COMPLEX REARRANGEMENT INVOLVING THREE AUTOSOMES IN A PHENOTYPICALLY NORMAL MALE PRESENTING WITH STERILITYTHOMAS IM.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 375-377; BIBL. 21 REF.Article

CHRONIC MYELOGENOUS LEUKEMIA WITH TRANSLOCATIONS (3Q-; 9Q+) AND (17Q-; 22Q+). POSSIBLE CRUCIAL CYTOGENETIC EVENTS IN THE GENESES OF CMLOSHIMURA M; OHYASHIKI K; VEHARA M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 48-51; BIBL. 21 REF.Article

CYTOGENETIC FOLLOW-UP OF PATIENTS WITH NONLYMPHOCYTIC LEUKEMIA. II: ACUTE NONLYMPHOCYTIC LEUKEMIAHAGEMEIJER A; KAHLEN K; ABELS J et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 2; PP. 109-124; BIBL. 19 REF.Article

TRISOMY 6 QTERTURLEAU C; DE GROUCHY J.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 3; PP. 202-206; BIBL. 9 REF.Article

OBSERVATION FAMILIALE DE TRISOMIE POUR LA PARTIE TERMINALE DU CHROMOSOME 10STOLL C; ROTH MP.1981; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1981; VOL. 38; NO 4; PP. 273-274; ABS. ENG; BIBL. 5 REF.Article

OCCURRENCE OF SEX CHROMOSOME MOSAICISM AND TRANSLOCATION DOWN'S SYNDROME IN THE SAME FAMILYSMITH A; ELLIOTT G.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 5; PP. 341-348; BIBL. 30 REF.Article

UNUSUAL TRANSLOCATION IN DOWN SYNDROMEFRYNS JP; DE WAEPENAERT E; VAN DEN BERGHE H et al.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; NO 1; PP. 47-49; BIBL. 4 REF.Article

RASSEGNA DI SETTE CASI DI PATOLOGIA AUTOSOMICA DI PUI RARO RISCONTRO: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1;21 = REVUE DE 7 CAS DE PATHOLOGIE AUTOSOMIQUE RARE: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1:21FIORETTI G; PAGANO L; RENDA S et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 12; PP. 807-814; ABS. ENG; BIBL. 4 REF.Article

A BALANCED TRANSLOCATION (17,22) AND A PERICENTRIC INVERSION OF CHROMOSOME 5: REPOSITORY IDENTIFICATION NO. GM3196TESTA JR; ROWLEY JD; HAWKINS C et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 4; PP. 270Article

A SUBTYPE OF THE PROTOTYPIC KARYOTYPE IN ACUTE MYELOID LEUKEMIA T (8; 21) (Q 22; Q 22), DEL 9 (Q 13; Q 23)HOSSFELD DK; HIGI M; KOEHLER S et al.1980; BLUT; DEU; DA. 1980; VOL. 40; NO 1; PP. 27-32; ABS. GER; BIBL. 17 REF.Article

ABSENCE OF LATE-REPLICATING X-CHROMOSOME IN A FEMALE PATIENT WITH ACUTE MYELOID LEUKEMIA AND THE 8; 21 TRANSLOCATIONLEVAN G; MITELMAN F.1979; J. NATION. CANCER INST.; USA; DA. 1979; VOL. 62; NO 2; PP. 273-275; BIBL. 9 REF.Article

The evolution of supernova remnants. I. Analysis of observational dataALLAKHVERDIYEV, A. O; AMNUEL, P. R; GUSEINOV, O. H et al.Astrophysics and space science. 1983, Vol 97, Num 2, pp 261-285, issn 0004-640XArticle

MOSAIC TETRASOMY 21 IN A LIVEBORN MALE INFANTHUNTER AGW; CLIFFORD B; SPEEVAK M et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 4; PP. 228-232; BIBL. 7 REF.Article

RED BLOOD CELL GLUTATHIONE PROXIDASE IN SIMPLE TRISOMY 21 AND TRANSLOCATION 21/22KEDZIORA J; LUKASZEWICZ R; KOTER M et al.1982; EXPERIENTIA; ISSN 0014-4754; CHE; DA. 1982; VOL. 38; NO 5; PP. 543-544; BIBL. 20 REF.Article

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