173 related articles for article (PubMed ID: 36991446)
21. Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY, -9, +DER(9)T(6:9)(p211:p24).
Eden MS; Thelin JW; Michalski K; Mitchell JA
Clin Genet; 1985 Nov; 28(5):375-84. PubMed ID: 4085142
[TBL] [Abstract][Full Text] [Related]
22. 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3).
Zhang YL; Dai Y; Tu ZG; Li QY
Cytogenet Genome Res; 2009; 127(1):67-72. PubMed ID: 20145385
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
[TBL] [Abstract][Full Text] [Related]
24. Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy.
Lenzini E; Drigo P; Redaelli S; Mammi I; Rosa-Rizzotto M; Dalprà L
Genet Test Mol Biomarkers; 2010 Oct; 14(5):695-701. PubMed ID: 20854099
[TBL] [Abstract][Full Text] [Related]
25. Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report.
Li R; Wang C; Zhang Z; Li D; Li L; Zhao D; Xu Z
BMC Pediatr; 2023 Apr; 23(1):168. PubMed ID: 37046298
[TBL] [Abstract][Full Text] [Related]
26. Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation.
Velinov M; Gu H; Yeboa K; Warburton D; Tubo T; Dhuper S; Lanter S; Delprino D; Kupchik G; Jenkins EC
Am J Med Genet; 2002 Feb; 107(4):330-3. PubMed ID: 11840491
[TBL] [Abstract][Full Text] [Related]
27. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation.
Hosono K; Kawase K; Kurata K; Niimi Y; Saitsu H; Minoshima S; Ohnishi H; Yamamoto T; Hikoya A; Tachibana N; Fukao T; Yamamoto T; Hotta Y
Ophthalmic Genet; 2020 Apr; 41(2):175-182. PubMed ID: 32223580
[No Abstract] [Full Text] [Related]
28. Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.
Martínez-Juárez A; Uribe-Figueroa L; Quintana-Palma M; Razo-Aguilera G; Sevilla-Montoya R
Cytogenet Genome Res; 2014; 142(4):249-54. PubMed ID: 24751616
[TBL] [Abstract][Full Text] [Related]
29. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
Stengel-Rutkowski S; Warkotsch A; Schimanek P; Stene J
Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
[TBL] [Abstract][Full Text] [Related]
30. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
Petković I; Barisić I; Bastić M; Hećimović S; Bago R
Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
[TBL] [Abstract][Full Text] [Related]
31. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
32. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE
Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787
[TBL] [Abstract][Full Text] [Related]
33. Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment.
Ardinger HH; Patil SR; Rhead WJ
Clin Genet; 1987 Jun; 31(6):381-5. PubMed ID: 3621640
[TBL] [Abstract][Full Text] [Related]
34. A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.
Assawamakin A; Wattanasirichaigoon D; Tocharoentanaphol C; Waeteekul S; Tansatit M; Thongnoppakhun W; Limwongse C
Am J Med Genet A; 2012 Apr; 158A(4):901-8. PubMed ID: 22419381
[TBL] [Abstract][Full Text] [Related]
35. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
Mishra R; Paththinige CS; Sirisena ND; Nanayakkara S; Kariyawasam UGIU; Dissanayake VHW
BMC Pediatr; 2018 Jan; 18(1):4. PubMed ID: 29310616
[TBL] [Abstract][Full Text] [Related]
36. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
Lyons MJ; Fuller JD; Montoya Mdel C; DuPont BR; Holden KR
J Child Neurol; 2013 Apr; 28(4):524-6. PubMed ID: 22752474
[TBL] [Abstract][Full Text] [Related]
37. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
[TBL] [Abstract][Full Text] [Related]
38. Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen.
Fritz B; Greber-Platzer S; Frischer T; Streubel B; Gröblacher J; Amann G; Ventruba P; Rehder H; Fonatsch C
Am J Med Genet; 2000 Oct; 94(4):271-80. PubMed ID: 11038438
[TBL] [Abstract][Full Text] [Related]
39. Familial distal monosomy 5p15.3-pter with trisomy 12q24.2-qter resulting in neurodevelopmental delay and dysmorphic features.
Čiuladaitė Ž; Matulevičienė A; Bandanskytė A; Brazaitis A; Kasnauskienė J; Kučinskas V
J Child Neurol; 2014 Mar; 29(3):399-405. PubMed ID: 23340083
[TBL] [Abstract][Full Text] [Related]
40. New chromosomal dysmorphic syndromes. 2. Trisomy 10p.
Stengel-Rutkowski S; Murken JD; Frankenberger R; Riechert M; Spiess H; Rodewald A; Stene J
Eur J Pediatr; 1977 Oct; 126(3):109-25. PubMed ID: 913435
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]