These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
151 related items for PubMed ID: 23608969
1. Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism. Frühmesser A, Erdel M, Duba HC, Fauth C, Amberger A, Utermann G, Zschocke J, Kotzot D. Eur J Med Genet; 2013 Jul; 56(7):383-8. PubMed ID: 23608969 [Abstract] [Full Text] [Related]
2. A new case of pure partial 7q duplication. Alfonsi M, Palka C, Morizio E, Gatta V, Franchi S, Guanciali Franchi P, Zori R, Calabrese G, Palka G, Chiarelli F. Cytogenet Genome Res; 2012 Jul; 136(1):1-5. PubMed ID: 22086126 [Abstract] [Full Text] [Related]
5. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies. Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L. Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299 [Abstract] [Full Text] [Related]
7. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3). Jeziorowska A, Ciesla W, Houck GE, Yao XL, Harris MS, Truszczak B, Skorski M, Jakubowski L, Jenkins EC, Kaluzewski B. Am J Med Genet; 1993 Apr 01; 46(1):83-7. PubMed ID: 7684191 [Abstract] [Full Text] [Related]
8. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability. Chen CP, Lin SP, Chern SR, Tsai FJ, Lee MS, Chen YJ, Wang W. Genet Couns; 2011 Apr 01; 22(4):425-30. PubMed ID: 22303804 [Abstract] [Full Text] [Related]
15. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder. Goumy C, Mihaescu M, Tchirkov A, Giollant M, Benier C, Francannet C, Jaffray JY, Geneix A, Vago P. Genet Couns; 2006 Apr 01; 17(3):371-9. PubMed ID: 17100206 [Abstract] [Full Text] [Related]