196 related articles for article (PubMed ID: 6683075)
1. Interstitial deletion 2q31 leads to q33.
Buchanan PD; Rhodes RL; Stevenson CE
Am J Med Genet; 1983 May; 15(1):121-6. PubMed ID: 6683075
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
Taysi K; Dengler DR; Jones LA; Heersma JR
Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
[No Abstract] [Full Text] [Related]
5. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
6. Monosomy 21: a possible stepwise evolution of the karyotype.
Abeliovich D; Carmi R; Karplus M; Bar-Ziv J; Cohen MM
Am J Med Genet; 1979; 4(3):279-86. PubMed ID: 574719
[TBL] [Abstract][Full Text] [Related]
7. Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation.
Nixon J; Oldridge M; Wilkie AO; Smith K
Am J Med Genet; 1997 Jun; 70(3):324-7. PubMed ID: 9188674
[TBL] [Abstract][Full Text] [Related]
8. Interstitial deletion 1p as a result of a de novo reciprocal 1p;2p translocation.
Hertz JM; Jensen PH
Ann Genet; 1985; 28(4):228-30. PubMed ID: 3879434
[TBL] [Abstract][Full Text] [Related]
9. [Del (13) (q33). Exclusion of esterase D (ESD) from 13q33 and q34].
Turleau C; Séger J; de Grouchy J; Doré F; Job JC
Ann Genet; 1978 Sep; 21(3):189-92. PubMed ID: 315197
[TBL] [Abstract][Full Text] [Related]
10. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
Boles RG; Pober BR; Gibson LH; Willis CR; McGrath J; Roberts DJ; Yang-Feng TL
Am J Med Genet; 1995 Jan; 55(2):155-60. PubMed ID: 7717414
[TBL] [Abstract][Full Text] [Related]
11. Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies.
Levin ML; Shaffer LG; Lewis RAp6 ; Gresik MV; Lupski JR
Am J Med Genet; 1995 Jan; 55(1):30-2. PubMed ID: 7702093
[TBL] [Abstract][Full Text] [Related]
12. [Intercalary deletions of 9q].
Turleau C; de Grouchy J; Chabrolle JP
Ann Genet; 1978 Dec; 21(4):234-6. PubMed ID: 314262
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
Chaabouni M; Martinovic J; Sanlaville D; Attié-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
[TBL] [Abstract][Full Text] [Related]
14. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
[TBL] [Abstract][Full Text] [Related]
15. An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.
Verheij JB; de Munnik SA; Dijkhuizen T; de Leeuw N; Olde Weghuis D; van den Hoek GJ; Rijlaarsdam RS; Thomasse YE; Dikkers FG; Marcelis CL; van Ravenswaaij-Arts CM
Eur J Med Genet; 2009; 52(5):353-7. PubMed ID: 19464398
[TBL] [Abstract][Full Text] [Related]
16. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
[TBL] [Abstract][Full Text] [Related]
17. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
[No Abstract] [Full Text] [Related]
18. 7q deletion syndrome (7q32 leads to 7qter).
Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
[TBL] [Abstract][Full Text] [Related]
19. Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.
Ramer JC; Mowrey PN; Robins DB; Ligato S; Towfighi J; Ladda RL
Am J Med Genet; 1990 Nov; 37(3):392-400. PubMed ID: 2260571
[TBL] [Abstract][Full Text] [Related]
20. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C
Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]