410 related articles for article (PubMed ID: 19372675)
1. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Liehr T; Stumm M; Wegner RD; Bhatt S; Hickmann P; Patsalis PC; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai WW; Cheung SW; Weise A
Cytogenet Genome Res; 2009; 124(1):102-5. PubMed ID: 19372675
[TBL] [Abstract][Full Text] [Related]
2. Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
Liehr T; Bartels I; Zoll B; Ewers E; Mrasek K; Kosyakova N; Merkas M; Hamid AB; von Eggeling F; Posorski N; Weise A
Cytogenet Genome Res; 2011; 132(1-2):121-3. PubMed ID: 20639618
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.
Mrasek K; Krüger G; Bauer I; Müller-Navia J; Liehr T; Weise A
Cytogenet Genome Res; 2008; 121(3-4):286-7. PubMed ID: 18758173
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
8. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
9. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
[TBL] [Abstract][Full Text] [Related]
10. Array comparative genomic hybridization in prenatal diagnosis: another experience.
Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
[TBL] [Abstract][Full Text] [Related]
11. Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
Mégarbané A; Gosset P; Souraty N; Lapierre JM; Korban R; Zahed L; Samaras L; Vekemans M; Prieur M
Am J Med Genet; 2001 Dec; 104(3):204-8. PubMed ID: 11754045
[TBL] [Abstract][Full Text] [Related]
12. Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Liehr T; Utine GE; Trautmann U; Rauch A; Kuechler A; Pietrzak J; Bocian E; Kosyakova N; Mrasek K; Boduroglu K; Weise A; Aktas D
Cytogenet Genome Res; 2007; 118(1):31-7. PubMed ID: 17901697
[TBL] [Abstract][Full Text] [Related]
13. Characterisation of supernumerary chromosomal markers: a study of 13 cases.
Douet-Guilbert N; Marical H; Pinson L; Herry A; Le Bris MJ; Morel F; De Braekeleer M
Cytogenet Genome Res; 2007; 116(1-2):18-23. PubMed ID: 17268173
[TBL] [Abstract][Full Text] [Related]
14. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
Lapierre JM; Cacheux V; Collot N; Da Silva F; Hervy N; Rivet D; Romana S; Wiss J; Benzaken B; Aurias A; Tachdjian G
Ann Genet; 1998; 41(3):133-40. PubMed ID: 9833066
[TBL] [Abstract][Full Text] [Related]
15. [Cytogenic characterization of chromosome markers detected at amniocentesis: implications for karyotype-phenotype correlations].
Valerio D; Aiello R; Altieri V; Antonucci F
Minerva Ginecol; 1996 Sep; 48(9):365-9. PubMed ID: 8999384
[TBL] [Abstract][Full Text] [Related]
16. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
[TBL] [Abstract][Full Text] [Related]
17. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
[TBL] [Abstract][Full Text] [Related]
18. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
Mercier S; Fellmann F; Cattin J; Bresson JL
Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
