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HABITUAL ABORTION AND TRANSLOCATION (22Q; 22Q): UNEXPECTED TRANSMISSION FROM A MOTHER TO HER PHENOTYPICALLY NORMAL DAUGHTERKIRKELS VGHJ; HUSTINX TWJ; SCHERES JMJC et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 456-461; BIBL. 23 REF.Article

Approche moléculaire des remaniements du chromosome 22 humain observés dans des pathologies tumorales non hématologiques: cas particulier de la t(11; 22) du Sarcome = Molecular approach of human chromosome 22 rearrangements observed in non hematologic tumoral pathologies with particular interest to the t(11; 22) Ewing's sarcoma specific translocationDelattre, Olivier; Thomas, Gilles.1991, 117 p.Thesis

Polymorphic bovine microsatellites INRAMTT178, INRAMTT180 and INRAMTT183VELMALA, R; BAIMAN, D; VIRTA, A et al.Animal genetics (Print). 1995, Vol 26, Num 3, pp 209-210, issn 0268-9146Article

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter → 22ql2.1 : Clinical, cytogenetic and molecular observationsVAGLIO, Alicia; MILUNSKY, Aubrey; HUANG, Xin-Li et al.European journal of medical genetics. 2008, Vol 51, Num 4, pp 332-342, issn 1769-7212, 11 p.Article

Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter→q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and Cat eyë phenotypical featuresGABARRON, J; GLOVER, G; JIMENEZ, A et al.Clinical genetics. 1985, Vol 28, Num 6, pp 509-515, issn 0009-9163Article

A first-generation linkage disequilibrium map of human chromosome 22DAWSON, Elisabeth; ABECASIS, Goncalo R; CARTER, David et al.Nature (London). 2002, Vol 418, Num 6897, pp 544-548, issn 0028-0836Article

Molecular and phenotypic characterization of ring chromosome 22JEFFRIES, Aaron R; CURRAN, Sarah; ELMSLIE, Frances et al.American journal of medical genetics. 2005, Vol 137A, Num 2, pp 139-147, issn 0148-7299, 9 p.Article

THE 11Q; 22Q TRANSLOCATION: A EUROPEAN COLLABORATIVE ANALYSIS OF 43 CASESFRACCARO M; LINDSTEN J; FORD CE et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 1; PP. 21-51; BIBL. 1 P.Article

PARTIAL TRISOMY OF 13 (PTER->Q12) DUE TO 47, XY,+DER (13), T(13; 22) (Q12; Q13)MATMOEDJONO SJ; SPARKES RS.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 241-246; BIBL. 19 REF.Article

Double trisomie et inversion péricentrique transmise [48,XXY, +21, inv(22)] effet interchrosomique = Double trisomy and inherited pericentric inversion [48,XXY, +21, inv(22)] interchromosomal effectSAURA, R; LONGY, M; SAUTAREL, M et al.Annales de génétique (Paris). 1983, Vol 26, Num 3, pp 180-182, issn 0003-3995Article

PARTIAL TRISOMY 13. THE MYTH OF NONMONGOLOID TRISOMY GPATIL SR; ZELLWEGER H.1981; CLIN. PEDIATR.; ISSN 0009-9228; USA; DA. 1981; VOL. 20; NO 8; PP. 534-536; BIBL. 15 REF.Article

Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphomaDIEN BARD, J; GELEBART, P; ANAND, M et al.Leukemia. 2008, Vol 22, Num 8, pp 1595-1603, issn 0887-6924, 9 p.Article

A CASE OF TRISOMY 22 IN PONGO PYGMAEUSANDRLE M; FIEDLER W; RETT A et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 1-6; BIBL. 17 REF.Article

Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30]NAKAMURA, Y; BALLARD, L; LEPPERT, M et al.Nucleic acids research. 1988, Vol 16, Num 12, issn 0305-1048, 5707Article

Catch 22 : Microdeletion 22q11 screening in patients with congenital heart defectsVON BEUST, G; BARTMUS, D; BARTELS, I et al.Genetic counseling. 1998, Vol 9, Num 3, pp 223-227, issn 1015-8146Conference Paper

DNA pooling and dense marker maps : a systematic search for genes for cognitive abilityHILL, L; CRAIG, I. W; CHORNEY, K et al.Neuroreport (Oxford). 1999, Vol 10, Num 4, pp 843-848, issn 0959-4965Article

Anesthesia in a patient with chromosome 11;22 translocation : a case report and literature reviewDRUM, Elizabeth T; HERLICH, Andrew; LEVINE, Bruce et al.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 11, pp 985-987, issn 1155-5645, 3 p.Article

Does chromosome 22 have anything to do with sex determination: Further studies on a 46, XX, 22q11.2 del maleERICKSON, Robert P; SKINNER, Steve; JACQUET, Hélène et al.American journal of medical genetics. 2003, Vol 123A, Num 1, pp 64-67, issn 0148-7299, 4 p.Article

A Family-and Population-Based Study of the UFD1L Gene for SchizophreniaLIN XIE; LIN YE; JUN WEI et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1076-1079, issn 1552-4841, 4 p.Article

Five new subjects with ring chromosome 22ISHMAEL, H. A; CATALDI, D; BEGLEITER, M. L et al.Clinical genetics. 2003, Vol 63, Num 5, pp 410-414, issn 0009-9163, 5 p.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

9;22;15 COMPLEX TRANSLOCATION IN PH1 CHROMOSOME POSITIVE CML REVEALED BY GIEMSA-11 PROCEDURE IN APPARENT LYMPHOID CELLS OF BLASTIC CRISISHAYS T; MORSE HG; ROBINSON A et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 4; PP. 283-292; BIBL. 16 REF.Article

Partial monosomy 15q due to de novo t(15; 22)(q15;p11)MORI, M. A; RODRIGUEZ, L; PINEL, I et al.Annales de génétique (Paris). 1987, Vol 30, Num 4, pp 246-248, issn 0003-3995Article

Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemiaVERMA, R. S; RODRIGUEZ, J; ARVIND BABU et al.Canadian journal of genetics and cytology. 1986, Vol 28, Num 6, pp 998-1002, issn 0008-4093Article

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

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