229 related articles for article (PubMed ID: 9298744)
1. Combined partial trisomy 3p/monosomy 5p resulting in sonographic abnormalities.
Entezami M; Coumbos A; Runkel S; Vogel M; Wegner R
Clin Genet; 1997 Aug; 52(2):96-9. PubMed ID: 9298744
[TBL] [Abstract][Full Text] [Related]
2. Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.
Goumy C; Beaufrère AM; Tchirkov A; Gouas L; Gaspard F; Giollant M; Roucaute T; Veronèse L; Lemery D; Vago P
Prenat Diagn; 2008 Feb; 28(2):131-4. PubMed ID: 18236428
[TBL] [Abstract][Full Text] [Related]
3. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
[TBL] [Abstract][Full Text] [Related]
4. Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).
Tsukuda T; Nagata I; Sawada H; Murakami J; Hanaki K; Urashima H; Kaneda T; Shimizu N; Kaibara N; Kodama N; Ohzeki T; Shiraki K
Clin Genet; 1996 Oct; 50(4):220-2. PubMed ID: 9001803
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
Chen CP; Liu FF; Jan SW; Lin SP; Lan CC
Prenat Diagn; 1996 Mar; 16(3):270-5. PubMed ID: 8710784
[TBL] [Abstract][Full Text] [Related]
6. Chromosomal abnormalities associated with a single umbilical artery.
Khong TY; George K
Prenat Diagn; 1992 Nov; 12(11):965-8. PubMed ID: 1494550
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations.
Chen CP; Chern SR; Tsai EJ; Lee CC; Chen LF; Wang W
Genet Couns; 2009; 20(3):281-8. PubMed ID: 19852436
[No Abstract] [Full Text] [Related]
8. Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.
Lai MM; Scriven PN; Ball C; Berry AC
J Med Genet; 1992 Aug; 29(8):586-8. PubMed ID: 1518027
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
[TBL] [Abstract][Full Text] [Related]
10. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
Balci S; Aypar E; Beksaç MS; Bartsch O
Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
[TBL] [Abstract][Full Text] [Related]
11. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
[TBL] [Abstract][Full Text] [Related]
12. Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.
de Carvalho AF; da Silva Bellucco FT; Kulikowski LD; Toralles MB; Melaragno MI
Hum Genet; 2008 Nov; 124(4):387-92. PubMed ID: 18777129
[TBL] [Abstract][Full Text] [Related]
13. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
de Almeida JC; Reis DF; Llerena JC; Pereira ET
Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
[TBL] [Abstract][Full Text] [Related]
14. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
Menéndez I; Casaña H
Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
[TBL] [Abstract][Full Text] [Related]
15. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
Frankova YE; Holenova H; Braulke I
Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
[TBL] [Abstract][Full Text] [Related]
16. Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
de Pater JM; Govaerts LC; de Man SA; van der Sijs-Bos CJ; Christiaens GC; van Dam WM; Loneus WH; Engelen JJ
Prenat Diagn; 2003 Sep; 23(9):747-51. PubMed ID: 12975787
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly.
Chen CP; Tzen CY; Chang TY; Lin CJ; Wang W; Lee CC; Town DD; Chen LF; Lee MS
Prenat Diagn; 2002 Dec; 22(12):1112-3. PubMed ID: 12454968
[No Abstract] [Full Text] [Related]
18. Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
Senses DA; Silan F; Uzun H; Alagöz D; Zafer C; Kocabay K; Karaüzüm SB; Cetin Z
Genet Couns; 2007; 18(2):163-70. PubMed ID: 17710868
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 3p and monosomy 5p diagnosed by spectral karyotyping (SKY).
Imataka G; Tsuboi T; Kuribayashi R; Miyamoto K; Ichikawa G; Suzumura H; Arisaka O
Genet Couns; 2013; 24(4):445-8. PubMed ID: 24551991
[No Abstract] [Full Text] [Related]
20. Cri du chat-syndrome in combination with partial trisomy 9 p.
Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
