146 related articles for article (PubMed ID: 6624439)
1. De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46,XY,del(2)(q12q14).
Antich J; Carbonell X; Mas J; Clusellas N
Acta Paediatr Scand; 1983 Jul; 72(4):631-3. PubMed ID: 6624439
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24).
Fryns JP; Van Bosstraeten B; Malbrain H; Van den Berghe H
Hum Genet; 1977 Nov; 39(2):233-8. PubMed ID: 598832
[TBL] [Abstract][Full Text] [Related]
3. De novo interstitial deletion del(1)(p21p32).
Bene M; Duca-Marinescu A; Ioan D; Maximilian C
J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
Al-Awadi SA; Farag TI; Usha R; el-Khalifa MY; Sundareshan TS; Al-Othman SA
Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the long arm of chromosome 3.
Martsolf JT; Ray M
Ann Genet; 1983; 26(2):98-9. PubMed ID: 6604494
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of chromosome 2 region in a malformed infant.
Melnyk AR; Muraskas J
Am J Med Genet; 1993 Jan; 45(1):49-51. PubMed ID: 8418659
[TBL] [Abstract][Full Text] [Related]
7. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA
Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997
[TBL] [Abstract][Full Text] [Related]
8. Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).
Fryns JP; Logghe N; Van Eygen M; Van Der Berghe H
Hum Genet; 1979 Apr; 48(1):127-30. PubMed ID: 457127
[TBL] [Abstract][Full Text] [Related]
9. A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.
Sichong Z; Bui TH; Castro I; Iselius L; Håkansson S; Lundmark KM
Hum Genet; 1981; 59(2):178-81. PubMed ID: 7327578
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities.
Widschwendter A; Riha K; Duba HC; Kreczy A; Marth C; Schwärzler P
Ultrasound Obstet Gynecol; 2002 Apr; 19(4):396-9. PubMed ID: 11952971
[TBL] [Abstract][Full Text] [Related]
11. De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter).
Yoshino M; Watanabe Y; Harada N; Abe K
J Med Genet; 1991 Aug; 28(8):539-40. PubMed ID: 1920371
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
Fryns JP; Kleczkowska A; Limbos C; Vandecasseye W; Van den Berghe H
Ann Genet; 1985; 28(4):248-50. PubMed ID: 3879440
[TBL] [Abstract][Full Text] [Related]
14. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
Gorski JL; Uhlmann WR; Glover TW
Am J Med Genet; 1990 Dec; 37(4):471-4. PubMed ID: 2260590
[TBL] [Abstract][Full Text] [Related]
15. De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report.
Sivasankaran S; Ho NK; Knight L
Ann Acad Med Singap; 1997 Jul; 26(4):507-9. PubMed ID: 9395821
[TBL] [Abstract][Full Text] [Related]
16. Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.
Stockton DW; Ross HL; Bacino CA; Altman CA; Shaffer LG; Lupski JR
Am J Med Genet; 1997 Aug; 71(2):189-93. PubMed ID: 9217220
[TBL] [Abstract][Full Text] [Related]
17. A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).
Higginbottom MC; Mascarello JT; Hassin H; McCord WK
J Med Genet; 1982 Feb; 19(1):71-3. PubMed ID: 7069751
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Deletion of the short arm of chromosome 3: a case report with necropsy findings.
Beneck D; Suhrland MJ; Dicker R; Greco MA; Wolman SR
J Med Genet; 1984 Aug; 21(4):307-10. PubMed ID: 6492097
[TBL] [Abstract][Full Text] [Related]
20. De novo del(3)(q2800).
Alvarez Arratia MC; Rivera H; Möller M; Valdivia A; Vigueras A; Cantu JM
Ann Genet; 1984; 27(2):109-11. PubMed ID: 6331786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]