140 related articles for article (PubMed ID: 7689326)
1. Terminal deletion of long arm of chromosome 4: patient report and literature review.
Evers LJ; Schrander-Stumpel CT; Engelen JJ; Mulder H; Borghgraef M; Fryns JP
Genet Couns; 1993; 4(2):139-45. PubMed ID: 7689326
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Deletion (9) (p13.1 p21.1).
Scaglia F; Bodamer OA; Berend SA; Adam LR; Shaffer LG
Am J Med Genet; 2000 Mar; 91(2):113-5. PubMed ID: 10748408
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
Fryburg JS; Golden WL
Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
[TBL] [Abstract][Full Text] [Related]
5. The 4q-Syndrome.
Strehle EM; Ahmed OA; Hameed M; Russell A
Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
[TBL] [Abstract][Full Text] [Related]
6. Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
Schrander-Stumpel CT; Govaerts LC; Engelen JJ; van der Blij-Philipsen M; Borghgraef M; Loots WJ; Peters JJ; Rijnvos WP; Smeets DF; Fryns JP
Am J Med Genet; 1994 May; 50(4):377-80. PubMed ID: 7516121
[TBL] [Abstract][Full Text] [Related]
7. Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).
Holden JJ; MacDonald EA
Am J Med Genet; 1985 Feb; 20(2):245-8. PubMed ID: 2579554
[TBL] [Abstract][Full Text] [Related]
8. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
[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. Del(4)(pter-->q33:) case report and review of the literature.
Grammatico P; Spaccini L; Di Rosa C; Cupilari F; Del Porto G
Genet Couns; 1997; 8(1):39-42. PubMed ID: 9101277
[TBL] [Abstract][Full Text] [Related]
11. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
Rauen KA; Albertson DG; Pinkel D; Cotter PD
Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
[TBL] [Abstract][Full Text] [Related]
12. Mild phenotype in interstitial 4p deletion: another patient and review of the literature.
Van de Graaf G; Sijstermans JM; Engelen JJ; Schrander-Stumpel CT
Genet Couns; 1997; 8(1):13-8. PubMed ID: 9101273
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
Fryns JP; Kleczkowska A; Van den Berghe H
Ann Genet; 1990; 33(1):43-5. PubMed ID: 2195980
[TBL] [Abstract][Full Text] [Related]
14. Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype.
Karnitis SA; Burns K; Sudduth KW; Golden WL; Wilson WG
Am J Med Genet; 1992 Sep; 44(2):153-7. PubMed ID: 1280909
[TBL] [Abstract][Full Text] [Related]
15. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
Sills ES; Burns MJ; Parker LD; Carroll LP; Kephart LL; Dyer CS; Papenhausen PR; Davis JG
Orphanet J Rare Dis; 2007 Feb; 2():9. PubMed ID: 17295911
[TBL] [Abstract][Full Text] [Related]
16. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
Wang TH; Johnston K; Hsieh CL; Dennery PA
Am J Med Genet; 1994 Feb; 49(4):399-401. PubMed ID: 8160733
[TBL] [Abstract][Full Text] [Related]
17. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
[TBL] [Abstract][Full Text] [Related]
18. Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and review.
van Bon BW; Koolen DA; Feenstra I; Neefs I; Pfundt R; Smeets DF; de Vries BB
Clin Dysmorphol; 2007 Oct; 16(4):279-82. PubMed ID: 17786124
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].
Schwartz S; Meekins J; Panny SR; Sun CC; Cohen MM
Am J Med Genet; 1983 May; 15(1):141-4. PubMed ID: 6859113
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
