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.
411 related articles for article (PubMed ID: 2573314)
1. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype. Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314 [TBL] [Abstract][Full Text] [Related]
2. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome. Fryns JP; Kleczkowska A; Decock P; Van den Berghe H Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981 [TBL] [Abstract][Full Text] [Related]
3. Further delineation of 7p trisomy. Case report and review of literature. Pallotta R; Dalprà L; Fusilli P; Zuffardi O Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888 [TBL] [Abstract][Full Text] [Related]
4. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223? van Buggenhout G; Decock P; Fryns JP Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089 [TBL] [Abstract][Full Text] [Related]
5. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature. de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364 [TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype. Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005 [TBL] [Abstract][Full Text] [Related]
7. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development. Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090 [TBL] [Abstract][Full Text] [Related]
8. [Trisomy 5p: a report of 2 cases]. Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955 [TBL] [Abstract][Full Text] [Related]
9. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15]. Fechtrup B; Kalhoff H; Diekmann L; Fritz B Klin Padiatr; 2000; 212(1):35-40. PubMed ID: 10719682 [TBL] [Abstract][Full Text] [Related]
10. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies. Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356 [TBL] [Abstract][Full Text] [Related]
11. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression]. Frankova YE; Holenova H; Braulke I Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961 [TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 15q: report of a patient and literature review. Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006 [TBL] [Abstract][Full Text] [Related]
13. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q? Riegel M; Schinzel A Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740 [TBL] [Abstract][Full Text] [Related]
14. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21). de Almeida JC; Reis DF; Llerena JC; Pereira ET Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779 [TBL] [Abstract][Full Text] [Related]
15. Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:). Fryns JP; Kleczkowska A; Vogels A; Van den Berghe H Ann Genet; 1989; 32(3):171-3. PubMed ID: 2573313 [TBL] [Abstract][Full Text] [Related]
16. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation. Cappon SL; Duncan AM; Khalifa MM Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374 [TBL] [Abstract][Full Text] [Related]
17. [Trisomy 4p. Mirror duplication of the short arm of chromosome 4 de novo]. Boyer JP; Andrieux L; Noel L; Mottet J Neuropsychiatr Enfance Adolesc; 1983 Jul; 31(7):319-21. PubMed ID: 6621831 [No Abstract] [Full Text] [Related]
18. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13. de Ravel T; Aerssens P; Vermeesch JR; Fryns JP Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232 [TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)). Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721 [TBL] [Abstract][Full Text] [Related]
20. Trisomy 9 mosaicism in a girl with multiple malformations. Diaz-Mares L; Molina B; Carnevale A Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]