133 related articles for article (PubMed ID: 11424139)
21. 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]
22. Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.
Cantú ES; Thomas IT; Frias JL
Clin Genet; 1989 Sep; 36(3):189-95. PubMed ID: 2676269
[TBL] [Abstract][Full Text] [Related]
23. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
24. Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient.
Juyal RC; Finucane B; Shaffer LG; Lupski JR; Greenberg F; Scott CI; Baldini A; Patel PI
Am J Med Genet; 1995 Nov; 59(3):406-7. PubMed ID: 8599375
[No Abstract] [Full Text] [Related]
25. Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13.
Dennis NR; Veltman MW; Thompson R; Craig E; Bolton PF; Thomas NS
Am J Med Genet A; 2006 Mar; 140(5):434-41. PubMed ID: 16470730
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
27. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
[TBL] [Abstract][Full Text] [Related]
28. Cytogenetic study of a severe case of Pallister-Killian syndrome using fluorescence in situ hybridization.
Gamal SM; Hasegawa T; Satoh H; Watanabe T; Endo K; Satoh Y
Jpn J Hum Genet; 1994 Jun; 39(2):259-67. PubMed ID: 8086644
[TBL] [Abstract][Full Text] [Related]
29. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
Chen CP; Chern SR; Chen YN; Chen SW; Wu PS; Yang CW; Lee CC; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
[TBL] [Abstract][Full Text] [Related]
33. A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.
Gimelli G; Giorda R; Beri S; Gimelli S; Zuffardi O
Eur J Med Genet; 2007; 50(4):264-73. PubMed ID: 17567547
[TBL] [Abstract][Full Text] [Related]
34. Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature.
Recalcati MP; Bonati MT; Beltrami N; Cardarelli L; Catusi I; Costa A; Garzo M; Mammi I; Mattina T; Nalesso E; Nardone AM; Postorivo D; Sajeva A; Varricchio A; Verri A; Villa N; Larizza L; Giardino D
Eur J Med Genet; 2018 Mar; 61(3):173-180. PubMed ID: 29174090
[TBL] [Abstract][Full Text] [Related]
35. Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review.
Warnier H; Barrea C; Bethlen S; Schrouff I; Harvengt J
Orphanet J Rare Dis; 2022 Apr; 17(1):174. PubMed ID: 35461249
[TBL] [Abstract][Full Text] [Related]
36. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
Bartsch O; Rasi S; Hoffmann K; Blin N
Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
[TBL] [Abstract][Full Text] [Related]
37. Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.
Eggermann K; Mau UA; Bujdosó G; Koltai E; Engels H; Schubert R; Eggermann T; Raff R; Schwanitz G
Clin Genet; 2002 Jul; 62(1):89-93. PubMed ID: 12123494
[TBL] [Abstract][Full Text] [Related]
38. Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl.
Lund HT; Tranebjaerg L
Acta Paediatr Scand; 1990; 79(6-7):714-8. PubMed ID: 2386070
[TBL] [Abstract][Full Text] [Related]
39. Tissue limited mosaicism in a patient with tetrasomy 9p.
Papenhausen P; Riscile G; Miller K; Kousseff B; Tedesco T
Am J Med Genet; 1990 Nov; 37(3):388-91. PubMed ID: 2260570
[TBL] [Abstract][Full Text] [Related]
40. Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant.
Vermeesch JR; Syrrou M; Salden I; Dhondt F; Matthijs G; Fryns JP
J Med Genet; 2002 Nov; 39(11):e72. PubMed ID: 12414834
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]