180 related articles for article (PubMed ID: 10323738)
1. Case of partial trisomy 9p and partial trisomy 14q resulting from a maternal translocation: overlapping manifestations of characteristic phenotypes.
Angle B; Yen F; Cole CW
Am J Med Genet; 1999 May; 84(2):132-6. PubMed ID: 10323738
[TBL] [Abstract][Full Text] [Related]
2. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
[TBL] [Abstract][Full Text] [Related]
3. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM
Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638
[TBL] [Abstract][Full Text] [Related]
4. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
Wang XR; Luo RL; Dai XH; Liu JY
Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
[TBL] [Abstract][Full Text] [Related]
5. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
Dundar M; Uzak A; Saatci C; Akalin H
Genet Couns; 2011; 22(3):287-92. PubMed ID: 22029170
[TBL] [Abstract][Full Text] [Related]
6. Partial trisomy 17q and monosomy 9p due to a familial translocation.
Cotter PD; Stewart NL
Ann Genet; 1990; 33(4):231-3. PubMed ID: 1710432
[TBL] [Abstract][Full Text] [Related]
7. Unusual phenotype in partial trisomy 14.
Lemire EG; Cardwell S
Am J Med Genet; 1999 Dec; 87(4):294-6. PubMed ID: 10588832
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
9. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.
Piram A; Ortolan D; Peres LC; Pina-Neto JM; Riegel M; Schinzel A
Am J Med Genet A; 2003 Jul; 120A(2):247-52. PubMed ID: 12833408
[TBL] [Abstract][Full Text] [Related]
10. The syndrome of partial trisomy 14q.
Lo Curto F; Maraschio P; Milanesi P; Severi F; Ugazio AC; Zuffardi O
Eur J Pediatr; 1976 Nov; 123(4):237-41. PubMed ID: 991871
[TBL] [Abstract][Full Text] [Related]
11. Calcification of basal ganglia in a patient with partial trisomy 5q and partial monosomy 18q.
Nakayama T; Sakakihara Y; Hanaoka S; Akagi K; Kamoshita S
Acta Paediatr Jpn; 1993 Aug; 35(4):340-4. PubMed ID: 8379328
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.
Cohen MM; Charrow J; Balkin NE; Harris CJ
Am J Hum Genet; 1983 Jul; 35(4):635-44. PubMed ID: 6881140
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
[TBL] [Abstract][Full Text] [Related]
15. Abnormal chromosome 9 in a neonate program. Report of three cases.
Nakamura Y; Sato E; Sakai K; Sakuma S; Hashimoto T; Sindou S
Arch Pathol Lab Med; 1990 Feb; 114(2):185-7. PubMed ID: 2302035
[TBL] [Abstract][Full Text] [Related]
16. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
Leichtman LG; Zackowski JL; Storto PD; Newlin A
Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
[TBL] [Abstract][Full Text] [Related]
17. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
Komatsu H; Kihara A; Komura E; Mitsufuji N; Tsujii H; Kakita S; Ikuta H
Genet Couns; 2001; 12(2):137-43. PubMed ID: 11491308
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation.
Van den Boogaard MJ; De Pater J; Hennekam RC
Genet Couns; 1991; 2(2):83-91. PubMed ID: 1781959
[TBL] [Abstract][Full Text] [Related]
20. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
