T(21Q21Q)/R(T(21Q21P)) MOSAIC IN TWO UNRELATED PATIENTS WITH MILD STIGMATA OF DOWN'S SYNDROMEDALLAPICCOLA B; BIANCO I; BRINCHI V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 56-58; ABS. ENG; BIBL. 4 REF.Article

Mosaic down's syndrome with de novo 45, XX, -21, -22, +t(21q; 22q)/46, XX, -21, +t(21q:21q) rearrangementTHARAPEL, A. T; REDHEENDRAN, R; MANKINEN, B et al.Journal of medical genetics. 1984, Vol 21, Num 5, pp 391-395, issn 0022-2593Article

TRISOMIE 21 PARTIELLE A 45 CHROMOSOMES PAR TRANSLOCATION DE DEUX 21 SUR LE 14: 45,XX,-14,-21,+T (14Q 21Q 21Q)EMBERGER JM; LLORET R; ROSSI D et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 3; PP. 179-180; ABS. ENG; BIBL. 5 REF.Article

A clinical report of a patient with two abnormal cell lines: 46,XX, del(21)(q22.1) and 47,XX, +3QUIGLEY, Denise I; SAILUS, Jeffery; KAISER-ROGERS, Kathleen et al.American journal of medical genetics. 2005, Vol 132A, Num 1, pp 101-105, issn 0148-7299, 5 p.Article

A RARE CASE OF MOSAIC DOWN SYNDROME 46, XY/46, XY, -21, +I(21Q)UCHIDA IA; WHELAN DT.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 4; PP. 271-274; BIBL. 10 REF.Article

AN INFANT WITH DUPLICATION OF 17Q21->17 QTERGALLIEN JU; NEU RL; WYNN RJ et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 1; PP. 111-115; BIBL. 2 REF.Article

Subtelomeric trisomy 21q : A new benign chromosomal variantBONAGLIA, Maria Clara; MARELLI, Susan; GOTTARDI, Giulietta et al.European journal of medical genetics. 2007, Vol 50, Num 1, pp 54-59, issn 1769-7212, 6 p.Article

TWO RECIPROCAL TRANSLOCATIONS T(QP+; 13Q-) AND T(13Q-; 21Q+): A STUDY OF THE FAMILIESPRIETO F; BADIA L; ASENSI F et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 7-11; BIBL. 15 REF.Article

Syndromic Mental Retardation With Thrombocytopenia Due to 21q22.11q22.12 Deletion: Report of Three PatientsKATZAKI, Eleni; MORIN, Gilles; MATHIEU-DRAMARD, Michèle et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 7, pp 1711-1717, issn 1552-4825, 7 p.Article

Pure proximal deletion of chromosome 21 and kyphosisKEREN, Boris; BEMARDIN, Céline; TOUTAIN, Annick et al.European journal of medical genetics. 2007, Vol 50, Num 6, pp 469-474, issn 1769-7212, 6 p.Article

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studiesEHLING, Daniela; KENNERKNECHT, Ingo; JUNGE, Annelore et al.American journal of medical genetics. 2004, Vol 131A, Num 3, pp 265-272, issn 0148-7299, 8 p.Article

PRENATAL DIAGNOSIS OF ISOCHROMOSOME 21p AND ISOCHROMOSOME 21q IN A FETUS WITH DOWN SYNDROMEYAKUT, S; SANHAL, C; MANGUOGLU, E et al.Genetic counseling. 2014, Vol 25, Num 3, pp 257-264, issn 1015-8146, 8 p.Article

AML1 gene amplification : a novel finding in childhood acute lymphoblastic leukemiaNIINI, T; KANERVA, J; VETTENRANTA, K et al.Haematologica (Roma). 2000, Vol 85, Num 4, pp 362-366, issn 0390-6078Article

Inherited 14q Duplication and 21q Deletion: A Rare Adjacent-2 Segregation in Multiple Family MembersDAVE, Bhavana J; OLNEY, Ann Haskins; ZALESKI, Dianna H et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 10, pp 2248-2253, issn 1552-4825, 6 p.Article

Microdeletion of the Down Syndrome Critical Region at 21q22FUJITA, Hideki; TORII, Chiharu; KOSAKI, Rika et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 4, pp 950-953, issn 1552-4825, 4 p.Article

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)CHEN, Chih-Ping; CHERN, Schu-Rern; LIN, Chyi-Chyang et al.Prenatal diagnosis. 2006, Vol 26, Num 4, pp 313-320, issn 0197-3851, 8 p.Article

Mental Retardation, Congenital Heart Malformation, and Myelodysplasia in a Patient With a Complex Chromosomal Rearrangement Involving the Critical Region 21q22MELIS, Daniela; GENESIO, Rita; CARELLA, Massimo et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 7, pp 1697-1705, issn 1552-4825, 9 p.Article