245 related articles for article (PubMed ID: 25263257)
1. De novo interstitial deletion 2q14.1q22.1: is there a recognizable phenotype?
Greally MT; Robinson E; Allen NM; O'Donovan D; Crolla JA
Am J Med Genet A; 2014 Dec; 164A(12):3194-202. PubMed ID: 25263257
[TBL] [Abstract][Full Text] [Related]
2. Chromosome 2 Interstitial Deletion (del(2)(q14.1q22.1) Syndrome With Novel Skeletal and Central Nervous System Features.
Albarakati R; Ababneh F; Alharbi M; Alzahrani RS; Almutairi MF
Cureus; 2023 Jan; 15(1):e33586. PubMed ID: 36636524
[TBL] [Abstract][Full Text] [Related]
3. A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features.
Der Kaloustian VM; Russell L; Aradhya S; Richard G; Rosenblatt B; Melançon S
Am J Med Genet A; 2011 Oct; 155A(10):2538-42. PubMed ID: 22043489
[TBL] [Abstract][Full Text] [Related]
4. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
Rauen KA; Albertson DG; Pinkel D; Cotter PD
Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
[TBL] [Abstract][Full Text] [Related]
5. 2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial features.
Chung BH; Stavropoulos J; Marshall CR; Weksberg R; Scherer SW; Yoon G
Am J Med Genet A; 2011 Feb; 155A(2):424-9. PubMed ID: 21271666
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.
Piccione M; Piro E; Serraino F; Cavani S; Ciccone R; Malacarne M; Pierluigi M; Vitaloni M; Zuffardi O; Corsello G
Eur J Med Genet; 2012 Apr; 55(4):238-44. PubMed ID: 22406401
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
Tzschach A; Krause-Plonka I; Menzel C; Knoblauch A; Toennies H; Hoeltzenbein M; Radke M; Ropers HH; Kalscheuer V
Am J Med Genet A; 2006 May; 140(10):1108-10. PubMed ID: 16619204
[TBL] [Abstract][Full Text] [Related]
8. Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.
Rea G; McCullough S; McNerlan S; Craig B; Morrison PJ
Eur J Med Genet; 2010; 53(3):162-7. PubMed ID: 20215058
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation.
Shanske AL; Edelmann L; Kardon NB; Gosset P; Levy B
Am J Med Genet A; 2004 Nov; 131(1):29-35. PubMed ID: 15368480
[TBL] [Abstract][Full Text] [Related]
11. A novel interstitial deletion of chromosome 2q21.1-q23.3: Case report and literature review.
Almuzzaini B; Alatwi NS; Alsaif S; Al Balwi MA
Mol Genet Genomic Med; 2020 Apr; 8(4):e1135. PubMed ID: 31989799
[TBL] [Abstract][Full Text] [Related]
12. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation.
Goumy C; Gay-Bellile M; Salaun G; Kemeny S; Eymard-Pierre E; Biard M; Pebrel-Richard C; Vanlieferinghen P; Francannet C; Tchirkov A; Laurichesse H; Rouzade C; Gouas L; Vago P
Birth Defects Res A Clin Mol Teratol; 2016 Sep; 106(9):793-7. PubMed ID: 27346851
[TBL] [Abstract][Full Text] [Related]
13. An interstitial deletion of chromosome 7 at band q21: a case report and review.
Courtens W; Vermeulen S; Wuyts W; Messiaen L; Wauters J; Nuytinck L; Peeters N; Storm K; Speleman F; Nöthen MM
Am J Med Genet A; 2005 Apr; 134A(1):12-23. PubMed ID: 15732063
[TBL] [Abstract][Full Text] [Related]
14. Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.
Chen CP; Lin SP; Chern SR; Chen YJ; Tsai FJ; Wu PC; Wang W
Eur J Med Genet; 2010; 53(4):217-20. PubMed ID: 20346423
[TBL] [Abstract][Full Text] [Related]
15. Deletion 2p15-16.1 syndrome: case report and review.
Prontera P; Bernardini L; Stangoni G; Capalbo A; Rogaia D; Romani R; Ardisia C; Dallapiccola B; Donti E
Am J Med Genet A; 2011 Oct; 155A(10):2473-8. PubMed ID: 21910216
[TBL] [Abstract][Full Text] [Related]
16. Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
Nagamani SC; Erez A; Eng C; Ou Z; Chinault C; Workman L; Coldwell J; Stankiewicz P; Patel A; Lupski JR; Cheung SW
Eur J Hum Genet; 2009 May; 17(5):573-81. PubMed ID: 19034313
[TBL] [Abstract][Full Text] [Related]
17. 2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?
Jaillard S; Dubourg C; Gérard-Blanluet M; Delahaye A; Pasquier L; Dupont C; Henry C; Tabet AC; Lucas J; Aboura A; David V; Benzacken B; Odent S; Pipiras E
J Med Genet; 2009 Dec; 46(12):847-55. PubMed ID: 18812405
[TBL] [Abstract][Full Text] [Related]
18. Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.
Kulharya AS; Flannery DB; Norris K; Lovell C; Levy B; Velagaleti GV
Am J Med Genet A; 2008 Sep; 146A(17):2234-41. PubMed ID: 18666229
[TBL] [Abstract][Full Text] [Related]
19. Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2).
Lalani SR; Sahoo T; Sanders ME; Peters SU; Bejjani BA
BMC Med Genet; 2006 Feb; 7():8. PubMed ID: 16472378
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization.
Klein OD; Cotter PD; Schmidt AM; Bick DP; Tidyman WE; Albertson DG; Pinkel D; Rauen KA
Am J Med Genet A; 2005 Nov; 138(4):349-54. PubMed ID: 16200635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
