135 related articles for article (PubMed ID: 11185078)
1. A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity.
Emberger W; Petek E; Plecko-Starting B; Kroisel PM; Zierler H; Wagner K
J Med Genet; 2000 Nov; 37(11):892-6. PubMed ID: 11185078
[No Abstract] [Full Text] [Related]
2. De novo complex chromosome rearrangement: a study of two patients.
Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
[TBL] [Abstract][Full Text] [Related]
3. Advanced paternal age and de-novo complex chromosomal rearrangement in offspring.
Benzacken B; Siffroi JP; Straub B; Le Bourhis C; Sauvion S; Gaudelus J; Dadoune JP; Wolf JP
Hum Reprod; 1998 Jul; 13(7):1801-3. PubMed ID: 9740427
[TBL] [Abstract][Full Text] [Related]
4. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
5. A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient.
Misceo D; Bjørgo K; Ormerod E; Ringen Ø; Rocchi M; van der Hagen CB; Frengen E
Am J Med Genet A; 2008 Dec; 146A(24):3230-3. PubMed ID: 19012337
[No Abstract] [Full Text] [Related]
6. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
[TBL] [Abstract][Full Text] [Related]
7. Deletion (2)(p14p15) in a child with severe neurodevelopmental delay.
Amir IM; Al-Tawil KI; Al-Hathal MM
J Med Genet; 2000 Sep; 37(9):E21. PubMed ID: 10978368
[No Abstract] [Full Text] [Related]
8. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features.
Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C
Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398
[TBL] [Abstract][Full Text] [Related]
9. Mental retardation, tall stature and minor phenotypic abnormalities associated with a de novo complex chromosome rearrangement.
De Brasi D; Della Casa R; Titomanlio L; D'Agostino A; Perone L; Andria G
Neuropediatrics; 2000 Jun; 31(3):164-6. PubMed ID: 10963108
[No Abstract] [Full Text] [Related]
10. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
[TBL] [Abstract][Full Text] [Related]
11. Subtelomeric rearrangements detected by FISH in three of 33 families with idiopathic mental retardation and minor physical anomalies.
Hélias-Rodzewicz Z; Bocian E; Stankiewicz P; Obersztyn E; Kostyk E; Jakubów-Durska K; Kutkowska-Kaźmierczak A; Mazurczak T
J Med Genet; 2002 Sep; 39(9):e53. PubMed ID: 12205123
[No Abstract] [Full Text] [Related]
12. Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.
Andries S; Sartenaer D; Rack K; Rombout S; Tuerlinckx D; Gillerot Y; Van Maldergem L
J Med Genet; 2002 Oct; 39(10):E60. PubMed ID: 12362042
[No Abstract] [Full Text] [Related]
13. Interstitial deletion of the long arm of chromosome 6.
Chery M; Formiga LF; Mujica P; André M; Stehelin D; Dozier C; Gilgenkrantz S
Ann Genet; 1989; 32(2):82-6. PubMed ID: 2757364
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22.
Mirza G; Imaizumi K; Ragoussis J
J Med Genet; 2000 Sep; 37(9):E22. PubMed ID: 10978369
[No Abstract] [Full Text] [Related]
15. A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomata.
Friling R; Yassur Y; Abeliovich D; Biedner B; Galil A; Dagan J; Carmi R
Ophthalmic Genet; 1995 Jun; 16(2):71-4. PubMed ID: 7493159
[TBL] [Abstract][Full Text] [Related]
16. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
Mercier S; Fellmann F; Cattin J; Bresson JL
Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics history.
Priya PK; Mishra VV; Liehr T; Ziegler M; Tiwari S; Patel A; Chettiar SS; Patel H
J Assist Reprod Genet; 2018 Apr; 35(4):721-725. PubMed ID: 29359264
[No Abstract] [Full Text] [Related]
19. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
