217 related articles for article (PubMed ID: 7747780)
1. Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicism.
Spinner NB; Grace KR; Owens NL; Sovinsky L; Pellegrino JE; McDonald-McGinn D; Zackai E
Am J Med Genet; 1995 Mar; 56(1):22-4. PubMed ID: 7747780
[TBL] [Abstract][Full Text] [Related]
2. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
3. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
[TBL] [Abstract][Full Text] [Related]
4. Disappearing trisomy 8 mosaicism.
Mark HF; Bier JA
Ann Clin Lab Sci; 1997; 27(4):293-8. PubMed ID: 9210975
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
Crowe CA; Schwartz S; Black CJ; Jaswaney V
Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic and molecular analysis in trisomy 12p.
Allen TL; Brothman AR; Carey JC; Chance PF
Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
[TBL] [Abstract][Full Text] [Related]
8. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
Kosaki R; Hanai S; Kakishima H; Okada MA; Hayashi S; Ito Y; Takahashi T; Kosaki K; Okuyama T
Congenit Anom (Kyoto); 2006 Jun; 46(2):115-7. PubMed ID: 16732770
[TBL] [Abstract][Full Text] [Related]
9. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
Schlegel M; Baumer A; Riegel M; Wiedemann U; Schinzel A
Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
[TBL] [Abstract][Full Text] [Related]
10. Partial mosaic trisomy 5: a new case report with ocular involvement.
Schlegel Z; Valent A; Hirsch A
J Fr Ophtalmol; 2009 Oct; 32(8):533-9. PubMed ID: 19664845
[TBL] [Abstract][Full Text] [Related]
11. Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.
de Pater J; Van der Sijs-Bos C; Prins M; Derks J; Albrechts J; Engelen J
Eur J Med Genet; 2006; 49(4):306-12. PubMed ID: 16461028
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability.
Jordan MA; Marques I; Rosendorff J; de Ravel TJ
Genet Couns; 1998; 9(2):139-46. PubMed ID: 9664211
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature.
Kaplan LC; Wayne A; Crowell S; Latt SA
Am J Med Genet; 1986 Apr; 23(4):925-30. PubMed ID: 3515939
[TBL] [Abstract][Full Text] [Related]
15. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Santos M; Mrasek K; Rigola MA; Starke H; Liehr T; Fuster C
Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694
[TBL] [Abstract][Full Text] [Related]
16. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
17. Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
Velissariou V; Antoniadi T; Gyftodimou J; Bakou K; Grigoriadou M; Christopoulou S; Hatzipouliou A; Donoghue J; Karatzis P; Katsarou E; Petersen MB
Eur J Hum Genet; 2002 Nov; 10(11):694-8. PubMed ID: 12404100
[TBL] [Abstract][Full Text] [Related]
18. Variable clinical expression of mosaic trisomy 16 in the newborn infant.
Devi AS; Velinov M; Kamath MV; Eisenfeld L; Neu R; Ciarleglio L; Greenstein R; Benn P
Am J Med Genet; 1993 Aug; 47(2):294-8. PubMed ID: 8213923
[TBL] [Abstract][Full Text] [Related]
19. Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome.
Avansino JR; Dennis TR; Spallone P; Stock AD; Levin ML
Am J Med Genet; 1999 Nov; 87(1):6-11. PubMed ID: 10528239
[TBL] [Abstract][Full Text] [Related]
20. Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosis.
Morava E; Czakó M; Aszmann M; Illés T; Kosztolányi GY
Genet Couns; 2002; 13(4):455-7. PubMed ID: 12558117
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
