74 related articles for article (PubMed ID: 17546703)
1. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Fickelscher I; Starke H; Schulze E; Ernst G; Kosyakova N; Mkrtchyan H; MacDermont K; Sebire N; Liehr T
Prenat Diagn; 2007 Aug; 27(8):783-5. PubMed ID: 17546703
[TBL] [Abstract][Full Text] [Related]
2. Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.
Slimani W; Jelloul A; Al-Rikabi A; Sallem A; Hasni Y; Chachia S; Ernez A; Chaieb A; Bibi M; Liehr T; Saad A; Mougou-Zerelli S
J Assist Reprod Genet; 2020 Jul; 37(7):1729-1736. PubMed ID: 32399795
[TBL] [Abstract][Full Text] [Related]
3. Somatic mosaicism in cases with small supernumerary marker chromosomes.
Liehr T; Karamysheva T; Merkas M; Brecevic L; Hamid AB; Ewers E; Mrasek K; Kosyakova N; Weise A
Curr Genomics; 2010 Sep; 11(6):432-9. PubMed ID: 21358988
[TBL] [Abstract][Full Text] [Related]
4. Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis.
Yang Y; Hao W
Mol Cytogenet; 2023 Sep; 16(1):23. PubMed ID: 37667392
[TBL] [Abstract][Full Text] [Related]
5. Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human.
Al-Rikabi ABH; Pekova S; Fan X; Jančušková T; Liehr T
Curr Genomics; 2018 Apr; 19(3):192-199. PubMed ID: 29606906
[TBL] [Abstract][Full Text] [Related]
6. Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.
Van Opstal D; Boter M; Noomen P; Srebniak M; Hamers G; Galjaard RJ
Mol Cytogenet; 2011 Jan; 4():2. PubMed ID: 21235775
[TBL] [Abstract][Full Text] [Related]
7. Small Supernumerary Marker Chromosomes in Human Infertility.
Armanet N; Tosca L; Brisset S; Liehr T; Tachdjian G
Cytogenet Genome Res; 2015; 146(2):100-108. PubMed ID: 26398339
[TBL] [Abstract][Full Text] [Related]
8. A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma.
Córdova-Fletes C; Domínguez MG; Vázquez-Cárdenas A; Figuera LE; Neira VA; Rojas-Martínez A; Ortiz-López R
Mol Syndromol; 2012 Sep; 3(3):131-135. PubMed ID: 23112755
[TBL] [Abstract][Full Text] [Related]
9. Be careful with small supernumerary marker chromosomes!
Rodríguez L
Front Genet; 2023; 14():1269679. PubMed ID: 37881803
[No Abstract] [Full Text] [Related]
10. Small supernumerary marker chromosomes derived from human chromosome 11.
Liehr T; Ziegler M; Person L; Kankel S; Padutsch N; Weise A; Weimer JP; Williams H; Ferreira S; Melo JB; Carreira IM
Front Genet; 2023; 14():1293652. PubMed ID: 38174048
[No Abstract] [Full Text] [Related]
11. Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review.
Liehr T; Al-Rikabi A
Front Genet; 2019; 10():1131. PubMed ID: 31781176
[TBL] [Abstract][Full Text] [Related]
12. Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.
Liehr T; Schreyer I; Kuechler A; Manolakos E; Singer S; Dufke A; Wilhelm K; Jančušková T; Čmejla R; Othman MAK; Al-Rikabi AH; Mrasek K; Ziegler M; Kankel S; Kreskowski K; Weise A
Mol Cytogenet; 2018; 11():20. PubMed ID: 29541160
[TBL] [Abstract][Full Text] [Related]
13. Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the
Brečević L; Rinčić M; Krsnik Ž; Sedmak G; Hamid AB; Kosyakova N; Galić I; Liehr T; Borovečki F
Transl Neurosci; 2015; 6(1):59-86. PubMed ID: 28123791
[TBL] [Abstract][Full Text] [Related]
14. Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.
Hochstenbach R; Nowakowska B; Volleth M; Ummels A; Kutkowska-Kaźmierczak A; Obersztyn E; Ziemkiewicz K; Gerloff C; Schanze D; Zenker M; Muschke P; Schanze I; Poot M; Liehr T
Mol Syndromol; 2016 Feb; 6(5):210-21. PubMed ID: 26997941
[TBL] [Abstract][Full Text] [Related]
15. Unrevealed mosaicism in the next-generation sequencing era.
Gajecka M
Mol Genet Genomics; 2016 Apr; 291(2):513-30. PubMed ID: 26481646
[TBL] [Abstract][Full Text] [Related]
16. Clinical impact of proximal autosomal imbalances.
Hamid A; Weise A; Voigt M; Bucksch M; Kosyakova N; Liehr T; Klein E
Balkan J Med Genet; 2012 Dec; 15(2):15-22. PubMed ID: 24052727
[TBL] [Abstract][Full Text] [Related]
17. Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.
Iourov IY; Vorsanova SG; Yurov YB
Curr Genomics; 2012 Sep; 13(6):477-88. PubMed ID: 23449087
[TBL] [Abstract][Full Text] [Related]
18. Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?
Guilherme RS; Klein E; Venner C; Hamid AB; Bhatt S; Melaragno MI; Volleth M; Polityko A; Kulpanovich A; Kosyakova N; Liehr T
Chromosome Res; 2012 Oct; 20(7):825-35. PubMed ID: 23076733
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
