La monosomie partielle du bras court du chromosome 12: au sujet d'une observation = The 12p partial monosomy: one caseBOILLY DARTIGALONGUE, B; PARENT, P; TOUDIC, L et al.Revue internationale de pédiatrie. 1985, Num 149, pp 5-10, issn 0048-8135Article

TRANSLOCATION T (2; 12) (P 25; Q21) CLASSEE D'ABORD COMME 2/XPASQUALI F; ZUFFARDI O; ZAMBONI G et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 64-66; ABS. ANGL.; BIBL. 12 REF.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

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 12 (P11;P13). REPORT OF A CASETENCONI R; BACCICHETTI C; ANGLANI F et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 95-98; ABS. FR.; BIBL. 13REF.Article

RING CHROMOSOME 12 AND LATENT CENTROMERESZUFFARDI O; DANESINO C; POLONI L et al.1980; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1980; VOL. 28; NO 3; PP. 151-157; BIBL. 24 REF.Article

Lethal presentation of mosaic tetrasomy 12p Pallister-Killian/syndromeYOUNG, I. D; DUCKETT, D. P; O'REILLY, K. M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 62-64, issn 0003-3995, 3 p.Article

Deletion (12) (q 15 q 21.2)WATSON, M. S; MCALLISTER-BARTON, L; MAHONEY, M. J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 343-344, issn 0022-2593, 2 p.Article

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

Involvement of chromosomes 7 and 12 in large bowell cancer: trisomy 7 and 12q = Atteinte des chromosomes 7 et 12 dans le cancer du gros intestin: trisomie 7 et 12qBECHER, R; GIBAS, Z; SANDBERG, A. A et al.Cancer genetics and cytogenetics. 1983, Vol 9, Num 4, pp 329-332, issn 0165-4608Article

Etude cytogénétique d'un cas de translocation balancée de novo des chromosomes 12 et 16CHENG ZAIYU; LIU CHUNYUN; GAO CHUNSHENG et al.Yíchuán xuébào. 1983, Vol 10, Num 5, pp 419-422, issn 0379-4172Article

PARTIAL TRISOMY 12QZABEL B; BAUMANN W.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 2; PP. 144-146; BIBL. 2 REF.Article

DELETION-TRANSLOCATION DEL(12)(P11)->T(10;12)(P13;P11)NIELSEN J; RASMUSSEN K; NIEBUHR E et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 53-55; ABS. FR.; BIBL. 36 REF.Article

LA TRISOMIE PARTIELLE DU BRAS COURT DU CHROMOSOME 12MEYER JEANNE.sd; FRA; METZ: DACTYLOGR. DUPLICATION ET RELIURE; DA. S.D.; 363; 86 P.: ILL.; 30 CM; BIBL. 7 P.; TH.: MED./NANCY 1/1978Thesis

SHORT ARM DELETION OF CHROMOSOME 12. REPORT OF TWO NEW CASES. = DELETION DU BRAS COURT DU CHROMOSOME 12. RAPPORT DE DEUX CASORYE E; CRAEN M.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 335-342; BIBL. 8 REF.Article

TRISOMIE 14Q PARTIELLE. II. TRISOMIE 14Q PARTIELLE PAR TRANSLOCATION MATERNELLE T(12; 14) (Q24.4; Q21)TURLEAU C; DE GROUCHY J; BOCQUENTIN F et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 41-44; ABS. ANGL.; BIBL. 8REF.Article

INVERSION PERICENTRIQUE DU 3, HOMOZYGOTE ET HETEROZYGOTE, ET TRANSLATION CENTROMERIQUE DU 12 DANS UNE FAMILLE D'ORANGS-OUTANGS. IMPLICATIONS EVOLUTIVESTURLEAU C; DE GROUCHY J; CHAVIN COLIN F et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 227-233; ABS. ANGL.; BIBL. 14 REF.Article

Intersitial del(12)(q15q22) in myelodysplastic syndromesFERRO, M. T; GARCIA-SAGREDO, J. M; RESINO, M et al.Cancer genetics and cytogenetics. 1995, Vol 80, Num 2, pp 158-159, issn 0165-4608Article

Chromosomal mosaicism in the Killian-Teschler-Nicola syndromeRAFFEL, L. J; MOHANDAS, T; RIMOIN, D. L et al.American journal of medical genetics. 1986, Vol 24, Num 4, pp 607-611, issn 0148-7299Article

Dissociation of a t(12; 21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12; 21) father?JUBERG, R. C; STALLARD, R; MOWREY, P et al.Human genetics. 1983, Vol 64, Num 3, pp 216-221, issn 0340-6717Article

Pallister-Killian syndrome : normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growning epidermal cells, but mosaic tetrasomy 12p in skin fibroblastsHORN, D; MAJEWSKI, F; HILDEBRANDT, B et al.Journal of medical genetics. 1995, Vol 32, Num 1, pp 68-71, issn 0022-2593Article

Distal 12p delection in a Stillborn infantBARONCINI, A; AVELLINI, C; NERI, C et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 358-360, issn 0148-7299, 3 p.Article

Partial monosomy 12 p 13.1→13.3ROMAIN, D. R; GOLDSMITH, J; COLUMBANO-GREEN, L. M et al.Journal of medical genetics. 1987, Vol 24, Num 7, pp 434-436, issn 0022-2593Article

Chromosome 12 rearrangement with breakage at the p11 level in hematologic disorders: report of four casesZACCARIA, A; ROSTI, G; TESTONI, N et al.Cancer genetics and cytogenetics. 1985, Vol 15, Num 3-4, pp 309-314, issn 0165-4608Article

A familial insertion involving an active nucleolar organiser within chromosome 12WATT, J. L; COUZIN, D. A; LLOYD, D. J et al.Journal of medical genetics. 1984, Vol 21, Num 5, pp 379-384, issn 0022-2593Article

KLINEFELTER'S SYNDROME WITH A 47,XXY,INV (12) (Q15Q24) KARYOTYPESINGH RP.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 3; PP. 189-190; BIBL. 4 REF.Article