137 related articles for article (PubMed ID: 21567909)
1. Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.
Breman AM; Probst FJ; Blazo MA; Schaaf CP; Roney EK; Craigen WJ; Bacino CA; Cheung SW
Am J Med Genet A; 2011 Jun; 155A(6):1465-8. PubMed ID: 21567909
[No Abstract] [Full Text] [Related]
2. A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.
Sahoo T; Naeem R; Pham K; Chheng S; Noblin ST; Bacino CA; Gambello MJ
Am J Med Genet A; 2005 Feb; 133A(1):93-8. PubMed ID: 15637724
[TBL] [Abstract][Full Text] [Related]
3. Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.
Wei J; Xie Y; He W; Liu W; Jian W; Chen M; Wang D; Wang X; Sun X
Cytogenet Genome Res; 2014; 144(4):294-8. PubMed ID: 25634515
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q.
Souraty N; Sanlaville D; Chédid R; Le Lorc'h M; Maurin ML; Ghanem L; Maalouf S; Vekemans M; Mégarbané A
Eur J Med Genet; 2007; 50(5):379-85. PubMed ID: 17716964
[TBL] [Abstract][Full Text] [Related]
5. [Isochromosome long arm 18].
Rodiere M; Donadio D; Emberger JM; Astruc J; Brunel D
Ann Pediatr (Paris); 1977 Sep; 24(8-9):611-6. PubMed ID: 16211915
[No Abstract] [Full Text] [Related]
6. Suspected gonadal mosaicism for isochromosomes 18p and 18q unsubstantiated by fluorescence in situ hybridization analysis of sperm.
Williams MS; Josephson KD; Gursoy N; Jackson-Cook C
Genet Med; 2001; 3(4):318-20. PubMed ID: 11478534
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype?
Maruotti GM; Fabbrini F; Napolitano R; Genesio R; Conti A; Mallia Milanes G; Mazzarelli LL; Martinelli P
Am J Med Genet A; 2011 Jan; 155A(1):225-7. PubMed ID: 21204237
[No Abstract] [Full Text] [Related]
8. i(18q) in amniotic and fetal cells with a normal karyotype in direct chorionic villus sampling: cytogenetics and pathology.
Levy-Mozziconacci A; Piquet C; Scheiner C; Adrai J; Potier A; Pelissier MC; Philip N
Prenat Diagn; 1996 Dec; 16(12):1156-9. PubMed ID: 8994254
[TBL] [Abstract][Full Text] [Related]
9. Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
Hwang KS; Pearson MA; Stankiewicz P; Lennon PA; Cooper ML; Wu J; Ou Z; Cai WW; Patel A; Cheung SW
Am J Med Genet A; 2005 Aug; 137(1):88-93. PubMed ID: 16015583
[TBL] [Abstract][Full Text] [Related]
10. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
van den Berg C; Pijpers L; Halley DJ; Opstal DV; Los FJ
Am J Med Genet; 1999 Sep; 86(2):151-5. PubMed ID: 10449651
[TBL] [Abstract][Full Text] [Related]
11. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
Von Beust G; Bartmus D; Bartels I
Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
[No Abstract] [Full Text] [Related]
12. Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome.
Versacci P; Digilio MC; Sauer U; Dallapiccola B; Marino B
Am J Med Genet A; 2005 Oct; 138A(2):185-6. PubMed ID: 16100728
[No Abstract] [Full Text] [Related]
13. Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.
Thienpont B; Gewillig M; Fryns JP; Devriendt K; Vermeesch J
Cytogenet Genome Res; 2006; 114(3-4):338-41. PubMed ID: 16954676
[TBL] [Abstract][Full Text] [Related]
14. A new patient with pure trisomy 4p resulting from isochromosome formation and whole arm translocation.
Zahed L; Oreibi G; El-Amine H; Obeid M; Bitar FF
Am J Med Genet A; 2004 Jul; 128A(1):60-2. PubMed ID: 15211659
[TBL] [Abstract][Full Text] [Related]
15. Pure trisomy 20p resulting from isochromosome formation and whole arm translocation.
Sidwell RU; Pinson MP; Gibbons B; Byatt SA; Svennevik EC; Hastings RJ; Flynn DM
J Med Genet; 2000 Jun; 37(6):454-8. PubMed ID: 10928855
[No Abstract] [Full Text] [Related]
16. Tetrasomy 18p caused by paternal meiotic nondisjunction.
Eggermann T; Engels H; Apacik C; Moskalonek B; Müller-Navia J; Schwanitz G; Stengel-Rutkowski S
Eur J Hum Genet; 1997; 5(3):175-7. PubMed ID: 9272743
[No Abstract] [Full Text] [Related]
17. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
Horbinski C; Carter EM; Heard PL; Sathanoori M; Hu J; Vockley J; Gunn S; Hale DE; Surti U; Cody JD
Am J Med Genet A; 2008 Nov; 146A(22):2898-904. PubMed ID: 18932219
[TBL] [Abstract][Full Text] [Related]
18. Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.
van Essen AJ; Schoots CJ; van Lingen RA; Mourits MJ; Tuerlings JH; Leegte B
Am J Med Genet; 1993 Aug; 47(1):85-8. PubMed ID: 8368259
[TBL] [Abstract][Full Text] [Related]
19. Toriello-Carey syndrome with a 6Mb interstitial deletion at 22q12 detected by array CGH.
Said E; Cuschieri A; Vermeesch J; Fryns JP
Am J Med Genet A; 2011 Jun; 155A(6):1390-2. PubMed ID: 21567913
[TBL] [Abstract][Full Text] [Related]
20. Two cases of isochromosome 18q syndrome.
Pal S; Siti MI; Ankathil R; Zilfalil BA
Singapore Med J; 2007 May; 48(5):e146-50. PubMed ID: 17453088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
