Two cases of ring chromosome 11ROMAIN, D. R; GEBBIE, O. B; PARFITT, R. G et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 380-382, issn 0022-2593Article

Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?BUHLER, E. M; BUHLER, U. K; CHRISTEN, R et al.Human genetics. 1983, Vol 64, Num 2, pp 163-166, issn 0340-6717Article

Langer-Giedion syndrome and deletion of the long arm of chromosome 8: confirmation of the critical segment to 8q23FRYNS, J. P; HEREMANS, G; MARIEN, J et al.Human genetics. 1983, Vol 64, Num 2, pp 194-195, issn 0340-6717Article

A LARGE PERICENTRIC INVERSION OF HUMAN CHROMOSOME 8HERVA R; DE LA CHAPELLE A.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 3; PP. 208-212; BIBL. 14 REF.Article

COAGULATION STUDIES IN PATIENTS WITH TRISOMY 8 SYNDROMESTENBJERG S; HUSTED S; BERNSEN A et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 241-242; ABS. FR.; BIBL. 4 REF.Article

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

FAMILIAL INVERSION OF CHROMOSOME NO. 8. AN AFFECTED CHILD AND A CARRIER FETUS = INVERSION FAMILIALE DU CHROMOSOME NO 8. UN ENFANT ATTEINT ET UN FOETUS CONDUCTEURFUJIMOTO A; WILSON MG; TOWNER JW et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 67-73; BIBL. 21REF.Article

AN (8; 12) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-213LIN CC; UCHIDA I; HOTZ H et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 78-79; BIBL. 1REF.Article

Deficiency of chromosome 8p21.1→4pter: case report and review of the literatureDOBYNS, W. B; DEWALD, G. W; CARLSON, R. O et al.American journal of medical genetics. 1985, Vol 22, Num 1, pp 125-134, issn 0148-7299Article

Malignant lymphomas with band 8q24 chromosome abnormality: a morphologic continuum extending from Burkitt's to immunoblastic lymphoma = Lymphomes malins avec anomalie de bande chromosomique 8924: une extension morphologique continue du Burkitt au lymphome immunoblastiqueSIGAUX, F; BERGER, R; BERNHEIM, A et al.British journal of haematology. 1984, Vol 57, Num 3, pp 393-405, issn 0007-1048Article

COMPLEX CHROMOSOMAL REARRANGEMENT: (YP+; 49-) TRANSLOCATION AND RING CHROMOSOME OF THE 49-CHROMOSOMEORYE E; CRAEN M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 47-49; ABS. FRE; BIBL. 8 REF.Article

CHROMOSOMAL PATTERNS IN A BENIGN HUMAN NEOPLASM, THE MIXED SALIVARY GLAND TUMOURMARK J; DAHLENFORS R; EKEDAHL C et al.1982; HEREDITAS; ISSN 0018-0661; SWE; DA. 1982; VOL. 96; NO 1; PP. 141-148; BIBL. 6 REF.Article

LETTER TO THE EDITOR: NO CHROMOSOME DELETION FOUND ON PROMETAPHASE BANDING IN TWO CASES OF LANGER-GIEDION SYNDROMEGORLIN RJ; CERVENKA J; BLOOM BA et al.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 3; PP. 347-348; BIBL. 10 REF.Article

KARYOTYPE-PHENOTYPE CORRELATION: MOSAIC TRISOMY 8 AND PARTIAL TRISOMIES OF DIFFERENT SEGMENTS OF CHROMOSOME 8.RICCARDI VM; CRANDALL BF; SCHINZEL A et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 363-367; BIBL. 17 REF.Article

A (2; 8) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. 6M-327.WORTON RG; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 243Article

FAMILIAL PERICENTRIC INVERSION OF CHROMOSOME 8: IS BREAKPOINT P22Q23 IMPORTANT IN THE FORMATION OF UNBALANCED RECOMBINANTSMOEDJONO SJ; SPARKES RS.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 4; PP. 235-237; ABS. FRE; BIBL. 6 REF.Article

PARTIAL 8P-SYNDROMEPATIL SR; HANSON JW.1980; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1980; VOL. 28; NO 4; PP. 123-129; ABS. FRE; BIBL. 12 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

PERICENTRIC INVERSION OF CHROMOSOME NO. 8.KAWANA S; WATANABE G; ASAMI T et al.1976; TOHOKU J. EXPER. MED.; JAP.; DA. 1976; VOL. 119; NO 1; PP. 65-70; BIBL. 15 REF.Article

A FAMILIAL PERICENTRIC INVERSION OF CHROMOSOME 8 ANALYSED WITH A HIGH RESOLUTION CHROMOSOME BANDING TECHNIQUETHE HUNG BUI; ZHANG SICHONG; CASTRO I et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 4; PP. 266-271; BIBL. 13 REF.Article

MOSAICISM FOR AN ADDITIONAL PARTIAL CHROMOSOME 8: 46,XX/47,XX+DER(8)(P21->QTER)PFEIFFER RA; KESSEL E; RATHGEN E et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 2; PP. 207-212; BIBL. 7 REF.Article

A FETUS WITH RECOMBINANT OF CHROMOSOME 8 INHERITED FROM HER CARRIER FATHER.FUJIMOTO A; TOWNER JW; TURKEL SB et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 40; NO 3; PP. 241-248; BIBL. 1 P. 1/2Article

DE NOVO BALANCED RECIPROCAL TRANSLOCATION 46,XY,T(6;8)(Q13;Q22).FRIED K; ROSENBLATT M; MUNDEL G et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 2; PP. 142-144; BIBL. 76 REF.Article