| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18698621 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 411 journal articles in the PubMed database | Email to a friend | | |
| Piccione M, Antona V, Piro E, et al.
10qter deletion: A new case. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 12.
Full Citation | Find Related Articles | | Petersen B, Strassburg HM, Feichtinger W, et al.
Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3. [Case Reports, Journal Article]
Am J Med Genet 1998 Apr 28; 77(1):60-2.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Martinet D, Filges I, Besuchet Schmutz N, et al.
Subtelomeric 6p deletion: Clinical and array-CGH characterization in two patients. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jul 15.
Abstract | Full Citation | Find Related Articles | | Ko WT, Lam WF, Lo FM, et al.
Wisconsin syndrome in a patient with interstitial deletion of the long arm of chromosome 3: further delineation of the phenotype. [Case Reports, Journal Article]
Am J Med Genet A 2003 Jul 30; 120(3):413-7.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kaalund SS, Møller RS, Tészás A, et al.
Investigation of 4q-deletion in two unrelated patients using array CGH. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 7.
Full Citation | Find Related Articles | | Shieh JT, Aradhya S, Novelli A, et al.
Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization. [Journal Article]
Am J Med Genet A 2006 Jun 15; 140(12):1267-73.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Chen CP, Wang TH, Lin SP, et al.
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism. [JOURNAL ARTICLE]
Eur J Med Genet 2006 May 15.
Abstract | Full Citation | Find Related Articles | | Mutesa L, Hellin AC, Jamar M, et al.
Precocious puberty associated with partial trisomy 18q and monosomy 11q. [Journal Article, Research Support, Non-U.S. Gov't]
Genet Couns 2007; 18(2):201-7.
Abstract | Full Citation | Find Related Articles | | Worthington S, Bower C, Harrop K, et al.
22q11 deletions in patients with conotruncal heart defects. [Journal Article]
J Paediatr Child Health 1998 Oct; 34(5):438-43.
Abstract | Full Citation | Find Related Articles |   |
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