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.
101 related articles for article (PubMed ID: 2958604)
1. Partial 1p monosomy in a physically and mentally retarded boy. Gencík A; Gencíkova A J Genet Hum; 1987 Aug; 35(4):309-15. PubMed ID: 2958604 [TBL] [Abstract][Full Text] [Related]
2. Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy. Gibbons B; Tan SY; Tam PY Singapore Med J; 1999 Apr; 40(4):273-5. PubMed ID: 10487083 [TBL] [Abstract][Full Text] [Related]
3. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3. Narahara K; Kikkawa K; Murakami M; Hiramoto K; Namba H; Tsuji K; Yokoyama Y; Kimoto H Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418 [TBL] [Abstract][Full Text] [Related]
4. [Terminal partial mosaic monosomy of the short arm of chromosome 3, in discordant monozygotic twins, 46,XY/46,XY, del (3) (p25)]. Bueno I; Olivares JL; Olmedillas MJ; Abad M; Bueno M An Esp Pediatr; 1987 Mar; 26(3):187-90. PubMed ID: 3579058 [TBL] [Abstract][Full Text] [Related]
5. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations. Milosević J; Kalicanin P J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357 [TBL] [Abstract][Full Text] [Related]
6. Partial monosomy for chromosome 22 in a girl with mental retardation. Yong YP; Knight LA; Yong MH; Lam S; Ho LY Singapore Med J; 1997 Feb; 38(2):85-6. PubMed ID: 9269370 [TBL] [Abstract][Full Text] [Related]
7. De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis. Reynolds JF; Wyandt HE; Kelly TE Am J Med Genet; 1985 Jan; 20(1):173-80. PubMed ID: 3970070 [TBL] [Abstract][Full Text] [Related]
8. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome. Lukusa T; van den Berghe L; Smeets E; Fryns JP Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161 [TBL] [Abstract][Full Text] [Related]
9. A case of interstitial 1q deletion [46,XY,del(q25q32.1)]. Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663 [TBL] [Abstract][Full Text] [Related]
10. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay. Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619 [TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases. Poissonnier M; Turleau C; Olivier-Martin M; Milleret-Proyart MJ; Prieur M; Dubos M; Cabanis MO; Mugneret F; Blanc P; Noel L Ann Genet; 1992; 35(3):146-51. PubMed ID: 1466563 [TBL] [Abstract][Full Text] [Related]
12. Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl. Morrison PJ; Jones J; Nevin NC Am J Med Genet; 1992 Mar; 42(5):678-80. PubMed ID: 1632437 [TBL] [Abstract][Full Text] [Related]
13. A specific syndrome due to deletion of the distal long arm of chromosome 1. Meinecke P; Vögtel D Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Interstitial deletion of long arm of chromosome 13. Carnevale A; Frias S; Alcantar R Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673 [TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl. Chen CP; Lin SP; Lee CC; Town DD; Wang W Genet Couns; 2006; 17(3):301-6. PubMed ID: 17100198 [TBL] [Abstract][Full Text] [Related]
17. Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidase. Frydman M; Steinberger J; Shabtai F; Steinherz R Am J Med Genet; 1986 Oct; 25(2):245-9. PubMed ID: 3096136 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotype. Van Buggenhout G; De Coen L; Fryns JP Ann Genet; 1998; 41(2):77-81. PubMed ID: 9706337 [TBL] [Abstract][Full Text] [Related]
19. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis. Blennow E; Bui TH; Wallin A; Kogner P Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743 [TBL] [Abstract][Full Text] [Related]
20. 18q- and 18q+ mosaicism in a mentally retarded boy. Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]