190 related articles for article (PubMed ID: 9738865)
1. Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products.
Zahed L; Der Kaloustian V; Batanian JR
Am J Med Genet; 1998 Aug; 79(1):30-4. PubMed ID: 9738865
[TBL] [Abstract][Full Text] [Related]
2. Balanced complex rearrangement involving chromosomes 8, 9, and 12 in a normal mother, derivative chromosome 9 with recombinant chromosome 12 in her daughter with minor anomalies.
Masuno M; Asano J; Yasuda K; Kondo T; Orii T
Am J Med Genet; 1993 Jan; 45(1):65-7. PubMed ID: 8418663
[TBL] [Abstract][Full Text] [Related]
3. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
[TBL] [Abstract][Full Text] [Related]
4. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
Röthlisberger B; Kotzot D; Brecevic L; Koehler M; Balmer D; Binkert F; Schinzel A
Eur J Hum Genet; 1999 Dec; 7(8):873-83. PubMed ID: 10602362
[TBL] [Abstract][Full Text] [Related]
5. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
[TBL] [Abstract][Full Text] [Related]
6. Two unbalanced segregation products due to a maternal t(7;16)inv(16).
Leegte B; Sikkema-Raddatz B; Hordijk R; Davelaar I; van der Veen A; Cobben JM
Prenat Diagn; 2001 Jul; 21(7):550-2. PubMed ID: 11494289
[TBL] [Abstract][Full Text] [Related]
7. Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.
Wenger SL; Sell SL; Painter MJ; Steele MW
Am J Med Genet; 1997 May; 70(2):150-4. PubMed ID: 9128934
[TBL] [Abstract][Full Text] [Related]
8. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
10. Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15).
Sawyer JR; Jones E; Hawks FF; Quirk JG; Cunniff C
Am J Med Genet; 1994 Feb; 49(4):422-7. PubMed ID: 8160737
[TBL] [Abstract][Full Text] [Related]
11. Two unusual chromosome aberrations ascertained by sonographic anomalies.
Bourthoumieu S; Esclaire F; Terro F; Fiorenza M; Eyraud JL; Servaud M; Cantaloube M; Fermeaux V; Yardin C
Prenat Diagn; 2004 Mar; 24(3):219-23. PubMed ID: 15057957
[TBL] [Abstract][Full Text] [Related]
12. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
13. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
Hoffman DJ; Punnett HH; Pyeritz RE
Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
[TBL] [Abstract][Full Text] [Related]
14. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
15. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
Wang H; McLaughlin M; Thompson C; Hunter AG
Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821
[TBL] [Abstract][Full Text] [Related]
16. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
17. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
Repetto GM; Wagstaff J; Korf BR; Knoll JH
Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
[TBL] [Abstract][Full Text] [Related]
18. Identical chromosome imbalance in two siblings born to a mother with a double reciprocal translocation.
Yardin C; Esclaire F; Gilbert B; Brosset P; Hugon J; Barthe D
Ann Genet; 1997; 40(4):232-4. PubMed ID: 9526620
[TBL] [Abstract][Full Text] [Related]
19. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
20. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]