228 related articles for article (PubMed ID: 8641683)
21. Interstitial deletion (6)q13q15.
Gershoni-Baruch R; Mandel H; Bar El H; Bar-Nizan N; Borochowitz Z; Dar H
Am J Med Genet; 1996 Apr; 62(4):345-7. PubMed ID: 8723062
[TBL] [Abstract][Full Text] [Related]
22. De novo "pure" partial trisomy (6)(p22.1-->pter) in a chromosome 15 with an enlarged satellite, identified by microdissection.
Engelen JJ; Marcelis CL; Alofs MG; Loneus WH; Pulles-Heintzberger CF; Hamers AJ
Am J Med Genet; 2001 Feb; 99(1):48-53. PubMed ID: 11170093
[TBL] [Abstract][Full Text] [Related]
23. Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature.
Zherebtsov MM; Klein RT; Aviv H; Toruner GA; Hanna NN; Brooks SS
Clin Dysmorphol; 2007 Jul; 16(3):135-140. PubMed ID: 17551325
[TBL] [Abstract][Full Text] [Related]
24. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
25. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
[TBL] [Abstract][Full Text] [Related]
26. Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.
Engelen JJ; Loots WJ; Albrechts JC; Motoh PC; Fryns JP; Hamers AJ; Geraedts JP
J Med Genet; 1996 Jul; 33(7):562-6. PubMed ID: 8818941
[TBL] [Abstract][Full Text] [Related]
27. Deletion of terminal portion of 6q: report of a case with unusual malformations.
Shen-Schwarz S; Hill LM; Surti U; Marchese S
Am J Med Genet; 1989 Jan; 32(1):81-6. PubMed ID: 2705486
[TBL] [Abstract][Full Text] [Related]
28. Deletion of chromosome 3q proximal region gives rise to a variable phenotype.
Mackie Ogilvie C; Rooney SC; Hodgson SV; Berry AC
Clin Genet; 1998 Mar; 53(3):220-2. PubMed ID: 9630079
[TBL] [Abstract][Full Text] [Related]
29. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
Spikes AS; Hegmann K; Smith JL; Shaffer LG
Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
[TBL] [Abstract][Full Text] [Related]
30. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
[TBL] [Abstract][Full Text] [Related]
31. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
[TBL] [Abstract][Full Text] [Related]
32. Expanding the clinical and neuroradiological phenotype of 6q27 microdeletion: olfactory bulb aplasia and anosmia.
Gerber JC; Neuhann TM; Tyshchenko N; Smitka M; Hackmann K
Am J Med Genet A; 2011 Aug; 155A(8):1981-6. PubMed ID: 21744487
[TBL] [Abstract][Full Text] [Related]
33. Deletion of the long arm of chromosome 6: two new patients and literature review.
Evers LJ; Schrander-Stumpel CT; Engelen JJ; Hoorntje TM; Pulles-Heintzberger CF; Schrander JJ; Albrechts JC; Peters J; Fryns JP
Clin Genet; 1996 Sep; 50(3):138-44. PubMed ID: 8946112
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes.
Viersbach R; Schwanitz G; Nöthen MM
Hum Genet; 1994 Jun; 93(6):663-7. PubMed ID: 8005590
[TBL] [Abstract][Full Text] [Related]
36. Terminal deletion 6p23: a case report.
Kormann-Bortolotto MH; Farah LM; Soares D; Corbani M; Müller R; Adell AC
Am J Med Genet; 1990 Dec; 37(4):475-7. PubMed ID: 2260591
[TBL] [Abstract][Full Text] [Related]
37. [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]
38. Clinical features in a case with ring chromosome 13.
Parcheta B; Wisniewski L; Piontek E; Szymanska J; Skawinski W; Wermenski K
Eur J Pediatr; 1985 Nov; 144(4):409-12. PubMed ID: 4076259
[TBL] [Abstract][Full Text] [Related]
39. Three cases with de novo 6q imbalance and variable prenatal phenotype.
Grati FR; Lalatta F; Turolla L; Cavallari U; Gentilin B; Rossella F; Cetin I; Antonazzo P; Bellotti M; Dulcetti F; Baldo D; Tenconi R; Simoni G; Miozzo M
Am J Med Genet A; 2005 Jul; 136(3):254-8. PubMed ID: 15957159
[TBL] [Abstract][Full Text] [Related]
40. Mechanism and genotype-phenotype correlation of two proximal 6q deletions characterized using mBAND, FISH, array CGH, and DNA sequencing.
Vlckova M; Trkova M; Zemanova Z; Hancarova M; Novotna D; Raskova D; Puchmajerova A; Drabova J; Zmitkova Z; Tan Y; Sedlacek Z
Cytogenet Genome Res; 2012; 136(1):15-20. PubMed ID: 22156400
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]