141 related articles for article (PubMed ID: 9457505)
21. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K
Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663
[TBL] [Abstract][Full Text] [Related]
22. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
23. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
[TBL] [Abstract][Full Text] [Related]
24. A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22.
Parruti G; Di Ilio C; Calabrese G; Stuppia L; Guanciali Franchi P; Aceto A; Palka G
Ann Genet; 1989; 32(1):55-8. PubMed ID: 2751250
[TBL] [Abstract][Full Text] [Related]
25. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
26. Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.
Münke M; Emanuel BS; Zackai EH
Am J Med Genet; 1988 Aug; 30(4):929-38. PubMed ID: 3055987
[TBL] [Abstract][Full Text] [Related]
27. Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting.
Ostroverkhova NV; Nazarenko SA; Rubtsov NB; Nazarenko LP; Bunina EN
Am J Med Genet; 1999 Nov; 87(3):217-20. PubMed ID: 10564873
[TBL] [Abstract][Full Text] [Related]
28. Clinical and molecular analyses of deletion 3p25-pter syndrome.
Mowrey PN; Chorney MJ; Venditti CP; Latif F; Modi WS; Lerman MI; Zbar B; Robins DB; Rogan PK; Ladda RL
Am J Med Genet; 1993 Jul; 46(6):623-9. PubMed ID: 8103286
[TBL] [Abstract][Full Text] [Related]
29. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
30. Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.
Potocki L; Chen KS; Park SS; Osterholm DE; Withers MA; Kimonis V; Summers AM; Meschino WS; Anyane-Yeboa K; Kashork CD; Shaffer LG; Lupski JR
Nat Genet; 2000 Jan; 24(1):84-7. PubMed ID: 10615134
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
33. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
34. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature.
Plomp AS; Schrander-Stumpel CT; Engelen JJ; Sijstermans JM; Loneus WH; Fryns JP
Genet Couns; 1995; 6(1):55-60. PubMed ID: 7794563
[TBL] [Abstract][Full Text] [Related]
35. Terminal deletion 4q in a severely retarded boy.
de Michelena MI; Campos PJ
Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
[TBL] [Abstract][Full Text] [Related]
36. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
Shimojima K; Páez MT; Kurosawa K; Yamamoto T
Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
[TBL] [Abstract][Full Text] [Related]
37. Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidase.
Frydman M; Steinberger J; Shabtai F; Steinherz R
Am J Med Genet; 1986 Oct; 25(2):245-9. PubMed ID: 3096136
[TBL] [Abstract][Full Text] [Related]
38. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
[TBL] [Abstract][Full Text] [Related]
39. Identification of chromosome 21 materials using the whole chromosome 21 specific library.
Isa MN; Boyd E; Turner TL; Tolmie J; Connor JM
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():92-5. PubMed ID: 8629150
[TBL] [Abstract][Full Text] [Related]
40. Characterization of marker chromosomes by fish using microdissected probes from old Carnoy-fixed cells: report of two cases.
Chinen Y; Tohma T; Izumikawa Y; Naritomi K; Hirayama K
Jpn J Hum Genet; 1997 Dec; 42(4):543-9. PubMed ID: 9560955
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]