211 related articles for article (PubMed ID: 16179230)
1. Narrowing the deleted region associated with the 15q21 syndrome.
Pramparo T; Mattina T; Gimelli S; Liehr T; Zuffardi O
Eur J Med Genet; 2005; 48(3):346-52. PubMed ID: 16179230
[TBL] [Abstract][Full Text] [Related]
2. The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.
Van Buggenhout G; Van Ravenswaaij-Arts C; Mc Maas N; Thoelen R; Vogels A; Smeets D; Salden I; Matthijs G; Fryns JP; Vermeesch JR
Eur J Med Genet; 2005; 48(3):276-89. PubMed ID: 16179223
[TBL] [Abstract][Full Text] [Related]
3. Mild mental retardation in a child with a de novo interstitial deletion of 15q21.2q22.1: a comparison with previously described cases.
Tempesta S; Sollima D; Ghezzo S; Politi V; Sinigaglia B; Balducci F; Celso B; Restuccia A; Stefani M; Cernetti R; Marzocchi C; Ciccone R; Zuffardi O; Bovicelli L; Santarini L
Eur J Med Genet; 2008; 51(6):639-45. PubMed ID: 18757045
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.
Klein OD; Cotter PD; Moore MW; Zanko A; Gilats M; Epstein CJ; Conte F; Rauen KA
Clin Genet; 2007 Mar; 71(3):260-6. PubMed ID: 17309649
[TBL] [Abstract][Full Text] [Related]
5. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
[TBL] [Abstract][Full Text] [Related]
6. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
Nagamani SC; Zhang F; Shchelochkov OA; Bi W; Ou Z; Scaglia F; Probst FJ; Shinawi M; Eng C; Hunter JV; Sparagana S; Lagoe E; Fong CT; Pearson M; Doco-Fenzy M; Landais E; Mozelle M; Chinault AC; Patel A; Bacino CA; Sahoo T; Kang SH; Cheung SW; Lupski JR; Stankiewicz P
J Med Genet; 2009 Dec; 46(12):825-33. PubMed ID: 19584063
[TBL] [Abstract][Full Text] [Related]
7. Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case.
Veredice C; Bianco F; Contaldo I; Orteschi D; Stefanini MC; Battaglia D; Lettori D; Guzzetta F; Zollino M
Epilepsia; 2009 Jul; 50(7):1810-5. PubMed ID: 19486360
[TBL] [Abstract][Full Text] [Related]
8. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
Rajcan-Separovic E; Harvard C; Liu X; McGillivray B; Hall JG; Qiao Y; Hurlburt J; Hildebrand J; Mickelson EC; Holden JJ; Lewis ME
J Med Genet; 2007 Apr; 44(4):269-76. PubMed ID: 16963482
[TBL] [Abstract][Full Text] [Related]
9. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
[TBL] [Abstract][Full Text] [Related]
10. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
Williams CA; Gray BA; Hendrickson JE; Stone JW; Cantú ES
Am J Med Genet; 1989 Mar; 32(3):339-45. PubMed ID: 2786338
[TBL] [Abstract][Full Text] [Related]
11. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
Redon R; Rio M; Gregory SG; Cooper RA; Fiegler H; Sanlaville D; Banerjee R; Scott C; Carr P; Langford C; Cormier-Daire V; Munnich A; Carter NP; Colleaux L
J Med Genet; 2005 Feb; 42(2):166-71. PubMed ID: 15689456
[No Abstract] [Full Text] [Related]
12. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
Kaplan LC; Wharton R; Elias E; Mandell F; Donlon T; Latt SA
Am J Med Genet; 1987 Sep; 28(1):45-53. PubMed ID: 3674117
[TBL] [Abstract][Full Text] [Related]
13. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
[TBL] [Abstract][Full Text] [Related]
14. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Van der Aa N; Rooms L; Vandeweyer G; van den Ende J; Reyniers E; Fichera M; Romano C; Delle Chiaie B; Mortier G; Menten B; Destrée A; Maystadt I; Männik K; Kurg A; Reimand T; McMullan D; Oley C; Brueton L; Bongers EM; van Bon BW; Pfund R; Jacquemont S; Ferrarini A; Martinet D; Schrander-Stumpel C; Stegmann AP; Frints SG; de Vries BB; Ceulemans B; Kooy RF
Eur J Med Genet; 2009; 52(2-3):94-100. PubMed ID: 19249392
[TBL] [Abstract][Full Text] [Related]
15. Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion.
Papadopoulou E; Sismani C; Christodoulou C; Ioannides M; Kalmanti M; Patsalis P
Am J Med Genet A; 2010 Jun; 152A(6):1515-22. PubMed ID: 20503328
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.
Ballarati L; Cereda A; Caselli R; Selicorni A; Recalcati MP; Maitz S; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2011; 54(1):55-9. PubMed ID: 20969981
[TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular characterization of a patient with 15q21.2q22.2 deletion syndrome.
Velázquez-Wong AC; Ruiz Esparza-Garrido R; Velázquez-Flores MÁ; Huicochea-Montiel JC; Cárdenas-Conejo A; Miguez-Muñoz CP; Araujo-Solís MA; Salamanca-Gómez F; Arenas-Aranda DJ
Cytogenet Genome Res; 2014; 144(3):183-9. PubMed ID: 25661042
[TBL] [Abstract][Full Text] [Related]
18. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
Davidsson J; Collin A; Olsson ME; Lundgren J; Soller M
Epilepsy Res; 2008 Sep; 81(1):69-79. PubMed ID: 18539002
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. An emerging phenotype of proximal 11q deletions.
Melis D; Genesio R; Cozzolino M; Del Giudice E; Mormile A; Imperati F; Ronga V; Della Casa R; Nitsch L; Andria G
Eur J Med Genet; 2010; 53(5):340-3. PubMed ID: 20688202
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
