228 related articles for article (PubMed ID: 15378554)
1. Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.
Demori E; Devescovi R; Benussi DG; Dolce S; Carrozzi M; Villa N; Miertus J; Amoroso A; Pecile V
Am J Med Genet A; 2004 Oct; 130A(3):288-94. PubMed ID: 15378554
[TBL] [Abstract][Full Text] [Related]
2. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
von Beust G; Sauter SM; Liehr T; Burfeind P; Bartels I; Starke H; von Eggeling F; Zoll B
Am J Med Genet A; 2005 Aug; 137(1):59-64. PubMed ID: 16007665
[TBL] [Abstract][Full Text] [Related]
3. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
[TBL] [Abstract][Full Text] [Related]
4. Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
Louvrier C; Egea G; Labalme A; Des Portes V; Gazzo S; Callet-Bauchu E; Till M; Sanlaville D; Edery P; Schluth-Bolard C
Cytogenet Genome Res; 2015; 147(2-3):111-7. PubMed ID: 26669311
[TBL] [Abstract][Full Text] [Related]
5. A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15.
Daniel A; Malafiej P
Am J Med Genet A; 2003 Mar; 117A(3):212-22. PubMed ID: 12599184
[TBL] [Abstract][Full Text] [Related]
6. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
7. Mosaic supernumerary r(8) syndrome.
Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
[No Abstract] [Full Text] [Related]
8. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
9. Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).
Blennow E; Annerén G; Bui TH; Berggren E; Asadi E; Nordenskjöld M
Am J Hum Genet; 1993 Aug; 53(2):433-42. PubMed ID: 8328459
[TBL] [Abstract][Full Text] [Related]
10. Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome.
Combi R; Sala E; Villa N; Crosti F; Beccaria L; Cogliardi A; Tenchini ML; Dalprà L
Clin Dysmorphol; 2008 Jan; 17(1):35-39. PubMed ID: 18049079
[TBL] [Abstract][Full Text] [Related]
11. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
Melnyk AR; Dewald G
Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
[TBL] [Abstract][Full Text] [Related]
12. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
Kumar MJ; Kumar RA; Subhashree V; Jayasudha T; Hemagowri V; Koshy T; Gowrishankar K
Cytogenet Genome Res; 2015; 146(2):120-123. PubMed ID: 26226839
[TBL] [Abstract][Full Text] [Related]
13. Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child.
Röthlisberger B; Zerova T; Kotzot D; Buzhievskaya TI; Balmer D; Schinzel A
J Med Genet; 2001 Dec; 38(12):885-8. PubMed ID: 11768396
[No Abstract] [Full Text] [Related]
14. Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.
van Langen IM; Otter MA; Aronson DC; Overweg-Plandsoen WC; Hennekam RC; Leschot NJ; Hoovers JM
Clin Genet; 1996 Jan; 49(1):49-53. PubMed ID: 8721573
[TBL] [Abstract][Full Text] [Related]
15. Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.
Anderlid BM; Sahlén S; Schoumans J; Holmberg E; Ahsgren I; Mortier G; Speleman F; Blennow E
Am J Med Genet; 2001 Mar; 99(3):223-33. PubMed ID: 11241494
[TBL] [Abstract][Full Text] [Related]
16. Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1 --> q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay.
Barbi G; Spaich Ch; Adolph S; Rossier E; Kehrer-Sawatzki H
Am J Med Genet A; 2005 Feb; 132A(4):419-24. PubMed ID: 15633178
[TBL] [Abstract][Full Text] [Related]
17. Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism.
Loeffler J; Soelder E; Erdel M; Utermann B; Janecke A; Duba HC; Utermann G
Am J Med Genet A; 2003 Jan; 116A(3):290-4. PubMed ID: 12503109
[TBL] [Abstract][Full Text] [Related]
18. Clinical findings in a patient mosaic for a supernumerary ring chromosome 20.
Austin-Ward ED; Castillo S; Dragnic Y; Sanz P; Salazar S; Knoll JH
Am J Med Genet; 2000 Mar; 91(3):171-4. PubMed ID: 10756336
[TBL] [Abstract][Full Text] [Related]
19. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
20. Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay.
Weimer J; Metzke-Heidemann S; Plendl H; Caliebe A; Grunewald R; Ounap K; Tammur P; Jonat W; Bartsch O; Siebert R; Arnold N
Am J Med Genet A; 2006 Mar; 140(5):488-95. PubMed ID: 16470789
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]