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1. Chen, CP; Chern, SR; Tzen, CY; Lee, MS; Pan, CW; Chang, TY; Wang, W
   Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts
   PRENATAL DIAGNOSIS
   
   C.P. Chen et al., "Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts", PRENAT DIAG, 21(4), 2001, pp. 317-320
2. Cotter, PD; Kaffe, S; Li, L; Gershin, IF; Hirschhorn, K
   Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   P.D. Cotter et al., "Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4", AM J MED G, 102(1), 2001, pp. 76-80
3. Birnbacher, R; Chudoba, I; Pirc-Danoewinata, H; Konig, M; Kohlhauser, C; Schnedl, W; Haas, OA
   Microdissection and reverse painting reveals a microdeletion 6(q26qter) ina de novo r(6) chromosome
   ANNALES DE GENETIQUE
   
   R. Birnbacher et al., "Microdissection and reverse painting reveals a microdeletion 6(q26qter) ina de novo r(6) chromosome", ANN GENET, 44(1), 2001, pp. 13-18
4. BOY R; PIMENTEL MMG; HEMERLY P; SILVA MDS; BARREIRO AP; DEALMEIDA JCC; LLERENA J
   CHROMOSOME 6Q DELETION - REPORT OF A NEW CASE AND REVIEW OF THE LITERATURE
   GENETICS AND MOLECULAR BIOLOGY
   
   R. Boy et al., "CHROMOSOME 6Q DELETION - REPORT OF A NEW CASE AND REVIEW OF THE LITERATURE", GENETICS AND MOLECULAR BIOLOGY, 21(1), 1998, pp. 145-149
5. WIECZOREK D; ENGELS H; VIERSBACH R; HENKE B; SCHWANITZ G; PASSARGE E
   ANALYSIS OF A FAMILIAL 3 WAY TRANSLOCATION INVOLVING CHROMOSOMES 3Q, 6Q, AND 15Q BY HIGH-RESOLUTION BANDING AND FLUORESCENT IN-SITU HYBRIDIZATION (FISH) SHOWS 2 DIFFERENT UNBALANCED KARYOTYPES IN SIBS
   Journal of Medical Genetics
   
   D. Wieczorek et al., "ANALYSIS OF A FAMILIAL 3 WAY TRANSLOCATION INVOLVING CHROMOSOMES 3Q, 6Q, AND 15Q BY HIGH-RESOLUTION BANDING AND FLUORESCENT IN-SITU HYBRIDIZATION (FISH) SHOWS 2 DIFFERENT UNBALANCED KARYOTYPES IN SIBS", Journal of Medical Genetics, 35(7), 1998, pp. 545-553
6. HOPKIN RJ; SCHORRY E; BOFINGER M; MILATOVICH A; STERN HJ; JAYNE C; SAAL HM
   NEW INSIGHTS INTO THE PHENOTYPES OF 6Q DELETIONS
   American journal of medical genetics
   
   R.J. Hopkin et al., "NEW INSIGHTS INTO THE PHENOTYPES OF 6Q DELETIONS", American journal of medical genetics, 70(4), 1997, pp. 377-386
7. RUBTSOV N; SENGER G; KUZCERA H; NEUMANN A; KELBOVA C; JUNKER K; BEENSEN V; CLAUSSEN U
   INTERSTITIAL DELETION OF CHROMOSOME 6Q - PRECISE DEFINITION OF THE BREAKPOINTS BY MICRODISSECTION DNA AMPLIFICATION, AND REVERSE PAINTING
   Human genetics
   
   N. Rubtsov et al., "INTERSTITIAL DELETION OF CHROMOSOME 6Q - PRECISE DEFINITION OF THE BREAKPOINTS BY MICRODISSECTION DNA AMPLIFICATION, AND REVERSE PAINTING", Human genetics, 97(6), 1996, pp. 705-709
8. WU BL; SCHNEIDER GH; SABATINO DE; BOZOVIC LZ; CAO B; KORF BR
   DISTAL 8P DELETION (8)(P23.1) - AN EASILY MISSED CHROMOSOMAL ABNORMALITY THAT MAY BE ASSOCIATED WITH CONGENITAL HEART DEFECT AND MENTAL-RETARDATION
   American journal of medical genetics
   
   B.L. Wu et al., "DISTAL 8P DELETION (8)(P23.1) - AN EASILY MISSED CHROMOSOMAL ABNORMALITY THAT MAY BE ASSOCIATED WITH CONGENITAL HEART DEFECT AND MENTAL-RETARDATION", American journal of medical genetics, 62(1), 1996, pp. 77-83
9. PANDYA A; BRAVERMAN N; PYERITZ RE; YING KL; KLINE AD; FALK RE
   INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-6 ASSOCIATED WITHUNUSUAL LIMB ANOMALIES - REPORT OF 2 NEW PATIENTS AND REVIEW OF THE LITERATURE
   American journal of medical genetics
   
   A. Pandya et al., "INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-6 ASSOCIATED WITHUNUSUAL LIMB ANOMALIES - REPORT OF 2 NEW PATIENTS AND REVIEW OF THE LITERATURE", American journal of medical genetics, 59(1), 1995, pp. 38-43
10. NEAVEL CB; SOUKUP S
    DELETION OF (11)(Q24.2) IN A MOTHER AND DAUGHTER WITH SIMILAR PHENOTYPES
    American journal of medical genetics
    
    C.B. Neavel e S. Soukup, "DELETION OF (11)(Q24.2) IN A MOTHER AND DAUGHTER WITH SIMILAR PHENOTYPES", American journal of medical genetics, 53(4), 1994, pp. 321-324
11. VALTAT C; GALLIANO D; METTEY R; TOUTAIN A; MORAINE C
    MONOSOMY-6Q - REPORT ON 4 NEW CASES
    Clinical genetics
    
    C. Valtat et al., "MONOSOMY-6Q - REPORT ON 4 NEW CASES", Clinical genetics, 41(3), 1992, pp. 159-166