173 related articles for article (PubMed ID: 7643363)
1. Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversion.
Prasher VP; Roberts E; Norman A; Butler AC; Krishnan VH; McMullan DJ
J Med Genet; 1995 Apr; 32(4):306-8. PubMed ID: 7643363
[TBL] [Abstract][Full Text] [Related]
2. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
[TBL] [Abstract][Full Text] [Related]
4. Inv21p12q22del21q22 and intellectual disability.
Oliveira R; Dória S; Madureira C; Lima V; Almeida C; Pinho MJ; Ramalho C; Matoso E; Barros A; Carreira IM; Moura CP
Gene; 2013 Mar; 517(1):120-4. PubMed ID: 23266646
[TBL] [Abstract][Full Text] [Related]
5. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
Ayral D; Raudrant D; Charleux JP; Noel B
Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
[TBL] [Abstract][Full Text] [Related]
6. A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.
Willatt LR; Davison BC; Goudie D; Alexander J; Dyson HM; Jenks PE; Ferguson-Smith ME
J Med Genet; 1992 Oct; 29(10):742-4. PubMed ID: 1433238
[TBL] [Abstract][Full Text] [Related]
7. [Phenotypic and genetic analysis of a boy with partial trisomy of 22q].
Zhang B; Xu Y; Kong J; Song Y; Li D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):532-534. PubMed ID: 32335879
[TBL] [Abstract][Full Text] [Related]
8. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations.
Mertens F; Johansson B; Forslund M; Olsson M; Kristoffersson U
Clin Genet; 1987 Jul; 32(1):46-8. PubMed ID: 3621653
[TBL] [Abstract][Full Text] [Related]
9. Eye findings in partial trisomy 2q.
Strömland K
Ophthalmic Paediatr Genet; 1985 Apr; 5(3):145-50. PubMed ID: 3934618
[TBL] [Abstract][Full Text] [Related]
10. Distal trisomy of chromosome 17q due to inverted tandem duplication.
Shimizu T; Ikeuchi T; Shinohara T; Ohba S; Miyaguchi H; Akiyama T; Shibata T
Clin Genet; 1988 Apr; 33(4):311-4. PubMed ID: 3359688
[TBL] [Abstract][Full Text] [Related]
11. A child with a recombinant of chromosome 8 inherited from her carrier mother.
Barnes IC; Kumar D; Bell RJ
J Med Genet; 1985 Feb; 22(1):67-70. PubMed ID: 3981583
[TBL] [Abstract][Full Text] [Related]
12. De novo inverted duplication 9p21pter involving telomeric repeated sequences.
Sanlaville D; Baumann C; Lapierre JM; Romana S; Collot N; Cacheux V; Turleau C; Tachdjian G
Am J Med Genet; 1999 Mar; 83(2):125-31. PubMed ID: 10190483
[TBL] [Abstract][Full Text] [Related]
13. Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation.
Gordon PL; Dalton JD; Martens PR; Tharapel AT; Wilroy RS
J Med Genet; 1993 May; 30(5):414-6. PubMed ID: 8320705
[TBL] [Abstract][Full Text] [Related]
14. A pericentric inversion of chromosome 9 and a rearrangement involving chromosomes 9 and 10, observed in two generations. Clinical description of chromosome 9 (p12-p21) deletion syndrome.
Fällström SP; Wahlström J
Clin Genet; 1979 Jun; 15(6):480-6. PubMed ID: 466847
[TBL] [Abstract][Full Text] [Related]
15. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
16. Costovertebral dysplasia in a patient with partial trisomy 22.
Tonk V; Wilson G; Schutt R; Mock J; Wyandt H; Mark HF; Ito M
Exp Mol Pathol; 2006 Apr; 80(2):197-200. PubMed ID: 16259976
[TBL] [Abstract][Full Text] [Related]
17. A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion.
Sgardioli IC; Simioni M; Viguetti-Campos NL; Prota JR; Gil-da-Silva-Lopes VL
Gene; 2013 Jul; 523(2):192-4. PubMed ID: 23566844
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2).
Tonk VS; Jesurun CA; Morgan DL; Lockhart LH; Velagaleti GV
Am J Med Genet A; 2004 Jan; 124A(1):92-5. PubMed ID: 14679594
[TBL] [Abstract][Full Text] [Related]
19. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
[TBL] [Abstract][Full Text] [Related]
20. Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature.
Douglas C; Smith SA; Rohena L
Am J Med Genet A; 2017 Jun; 173(6):1673-1680. PubMed ID: 28394407
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
