204 related articles for article (PubMed ID: 10797426)
21. [Inverted duplication of the short arm of chromosome 8].
Rodríguez Martínez L; Jiménez Muñoz-Delgado N; Nieto C; Martínez Carrascal A; López Grondona F; Martínez Frías ML
An Esp Pediatr; 2001 Nov; 55(5):458-62. PubMed ID: 11696311
[TBL] [Abstract][Full Text] [Related]
22. Analphoid 3qter markers.
Teshima I; Bawle EV; Weksberg R; Shuman C; Van Dyke DL; Schwartz S
Am J Med Genet; 2000 Sep; 94(2):113-9. PubMed ID: 10982967
[TBL] [Abstract][Full Text] [Related]
23. Construction of YAC-based mammalian artificial chromosomes.
Ikeno M; Grimes B; Okazaki T; Nakano M; Saitoh K; Hoshino H; McGill NI; Cooke H; Masumoto H
Nat Biotechnol; 1998 May; 16(5):431-9. PubMed ID: 9592390
[TBL] [Abstract][Full Text] [Related]
24. Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
Schrander-Stumpel CT; Govaerts LC; Engelen JJ; van der Blij-Philipsen M; Borghgraef M; Loots WJ; Peters JJ; Rijnvos WP; Smeets DF; Fryns JP
Am J Med Genet; 1994 May; 50(4):377-80. PubMed ID: 7516121
[TBL] [Abstract][Full Text] [Related]
25. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
[TBL] [Abstract][Full Text] [Related]
26. Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels.
Fisher AM; Barber JC; Crolla JA; James RS; Lestas AN; Jennings I; Dennis NR
Am J Med Genet; 1993 Aug; 47(1):100-5. PubMed ID: 8368238
[TBL] [Abstract][Full Text] [Related]
27. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
Hu J; McPherson E; Surti U; Hasegawa SL; Gunawardena S; Gollin SM
Am J Med Genet; 2002 Nov; 113(1):82-8. PubMed ID: 12400070
[TBL] [Abstract][Full Text] [Related]
28. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
29. Interstitial deletion of proximal 8q including part of the centromere from unbalanced segregation of a paternal deletion/marker karyotype with neocentromere formation at 8p22.
Burnside RD; Ibrahim J; Flora C; Schwartz S; Tepperberg JH; Papenhausen PR; Warburton PE
Cytogenet Genome Res; 2011; 132(4):227-32. PubMed ID: 21212645
[TBL] [Abstract][Full Text] [Related]
30. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
31. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
[TBL] [Abstract][Full Text] [Related]
32. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
[TBL] [Abstract][Full Text] [Related]
33. A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere.
Lo AW; Craig JM; Saffery R; Kalitsis P; Irvine DV; Earle E; Magliano DJ; Choo KH
EMBO J; 2001 Apr; 20(8):2087-96. PubMed ID: 11296241
[TBL] [Abstract][Full Text] [Related]
34. An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection.
Mahjoubi F; Peters GB; Malafiej P; Shalhoub C; Turner A; Daniel A; Hill RJ
Cytogenet Genome Res; 2005; 109(4):485-90. PubMed ID: 15905642
[TBL] [Abstract][Full Text] [Related]
35. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
Knight LA; Lipson M; Mann J; Bachman R
Am J Med Genet; 1984 Mar; 17(3):649-54. PubMed ID: 6585144
[TBL] [Abstract][Full Text] [Related]
36. A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?
Voullaire LE; Slater HR; Petrovic V; Choo KH
Am J Hum Genet; 1993 Jun; 52(6):1153-63. PubMed ID: 7684888
[TBL] [Abstract][Full Text] [Related]
37. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
[TBL] [Abstract][Full Text] [Related]
38. Marker chromosome 21 identified by microdissection and FISH.
Sun Y; Rubinstein J; Soukup S; Palmer CG
Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
[TBL] [Abstract][Full Text] [Related]
39. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
Vermeesch JR; Melotte C; Salden I; Riegel M; Trifnov V; Polityko A; Rumyantseva N; Naumchik I; Starke H; Matthijs G; Schinzel A; Fryns JP; Liehr T
Eur J Med Genet; 2005; 48(3):319-27. PubMed ID: 16179227
[TBL] [Abstract][Full Text] [Related]
40. A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.
Eussen BH; van de Laar I; Douben H; van Kempen L; Hochstenbach R; De Man SA; Van Opstal D; de Klein A; Poddighe PJ
Eur J Med Genet; 2007; 50(2):112-9. PubMed ID: 17161033
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]