193 related articles for article (PubMed ID: 2573313)
1. 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]
2. 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]
3. Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.
Wu BL; Schneider GH; Sabatino DE; Bozovic LZ; Cao B; Korf BR
Am J Med Genet; 1996 Mar; 62(1):77-83. PubMed ID: 8779331
[TBL] [Abstract][Full Text] [Related]
4. Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.
Devriendt K; De Mars K; De Cock P; Gewillig M; Fryns JP
Ann Genet; 1995; 38(4):228-30. PubMed ID: 8629811
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
Davies J; Voullaire L; Bankier A
Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
Barber JC; James RS; Patch C; Temple IK
Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
[TBL] [Abstract][Full Text] [Related]
8. Deletion of 2p: a cytogenetic and clinical update.
Neidich J; Zackai E; Aronson M; Emanuel BS
Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
[TBL] [Abstract][Full Text] [Related]
9. Small terminal deletions of the long arm of chromosome 2: two new cases.
Fisher AM; Ellis KH; Browne CE; Barber JC; Barker M; Kennedy CR; Foley H; Patton MA
Am J Med Genet; 1994 Dec; 53(4):366-9. PubMed ID: 7532357
[TBL] [Abstract][Full Text] [Related]
10. Tricho-rhino-phalangeal syndrome type II (Langer-Giedion) with persistent cloaca and prune belly sequence in a girl with 8q interstitial deletion.
Ramos FJ; McDonald-McGinn DM; Emanuel BS; Zackai EH
Am J Med Genet; 1992 Dec; 44(6):790-4. PubMed ID: 1481848
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
de Almeida JC; Reis DF; Martins RR
Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
[TBL] [Abstract][Full Text] [Related]
14. Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.
McMilin KD; Reiss JA; Brown MG; Black MH; Buckmaster DA; Durum CT; Gunter KA; Lawce HJ; Berry TL; Lamb OA; Olson CL; Weeks FF; Yoshitomi MJ; Jacky PB; Olson SB; Magenis RE
Am J Med Genet; 1998 Jun; 78(1):36-43. PubMed ID: 9637421
[TBL] [Abstract][Full Text] [Related]
15. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
Chen CP; Lin SP; Chern SR; Lee CC; Chen LF; Chen YJ; Wang W
Genet Couns; 2006; 17(1):81-5. PubMed ID: 16719283
[No Abstract] [Full Text] [Related]
16. Interstitial deletion of chromosome 2 (p23p25).
Penchaszadeh VB; Dowling PK; Davis JG; Schmidt R; Wapnir RA
Am J Med Genet; 1987 Jul; 27(3):701-6. PubMed ID: 3477099
[TBL] [Abstract][Full Text] [Related]
17. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
[TBL] [Abstract][Full Text] [Related]
18. [Interstitial deletion of the long arms of chromosome 13].
Molina M; Santolaya JM; Onaindía ML; Sánchez E; De Gárate J
An Esp Pediatr; 1982 Apr; 16(4):346-51. PubMed ID: 7125394
[TBL] [Abstract][Full Text] [Related]
19. Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
Brown S; Gersen S; Anyane-Yeboa K; Warburton D
Am J Med Genet; 1993 Jan; 45(1):52-9. PubMed ID: 8418661
[TBL] [Abstract][Full Text] [Related]
20. Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardation.
Felbor U; Knötgen N; Schams G; Buwe A; Steinlein C; Schmid M
Cytogenet Genome Res; 2004; 106(1):55-60. PubMed ID: 15218242
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]