158 related articles for article (PubMed ID: 6982665)
41. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
Ferrante E; Vignetti P; Antonelli M; Bruni L; Bertasi S; Chessa L
Helv Paediatr Acta; 1983 Mar; 38(1):73-80. PubMed ID: 6345474
[TBL] [Abstract][Full Text] [Related]
42. Langer-Giedion syndrome with interstitial 8q-deletion.
Zabel BU; Baumann WA
Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
[TBL] [Abstract][Full Text] [Related]
43. Constitutional del(5)(q23.3q31.1).
Rivera H; Garcia-Esquivel L; Moller M; Cantú JM
Ann Genet; 1987; 30(2):91-3. PubMed ID: 3499848
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal.
Fryns JP; Kleczkowska A; Casaer P; van den Berghe H
Ann Genet; 1986; 29(1):49-52. PubMed ID: 3487277
[TBL] [Abstract][Full Text] [Related]
46. Interstitial del(13q) associated with blindness and mental retardation.
Juberg RC; Mowrey PN
Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
[TBL] [Abstract][Full Text] [Related]
47. 18q- and 18q+ mosaicism in a mentally retarded boy.
Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
[TBL] [Abstract][Full Text] [Related]
48. Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.
Utine GE; Aktas D; Boduroğlu K; Alikasifoğlu M; Tunçbilek E
Genet Couns; 2007; 18(2):171-7. PubMed ID: 17710869
[TBL] [Abstract][Full Text] [Related]
49. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
[TBL] [Abstract][Full Text] [Related]
50. Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
Brown S; Gersen S; Anyane-Yeboa K; Warburton D
Am J Med Genet; 1993 Jan; 45(1):52-9. PubMed ID: 8418661
[TBL] [Abstract][Full Text] [Related]
51. Partial 9p monosomy--a case with hypothyroidism.
Ioan D; Dumitriu L; Muşeţeanu P; Bereliuc L; Belengeanu V; Maximilian C
Endocrinologie; 1985; 23(4):279-81. PubMed ID: 4089505
[TBL] [Abstract][Full Text] [Related]
52. Monosomy 1p36 deletion syndrome.
Gajecka M; Mackay KL; Shaffer LG
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
[TBL] [Abstract][Full Text] [Related]
53. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
54. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
Sills JA; Buckton KE; Raeburn JA
J Med Genet; 1976 Dec; 13(6):507-10. PubMed ID: 1018309
[TBL] [Abstract][Full Text] [Related]
57. Multiple critical smallest region of overlap in monosomy 16Q syndrome?
Doco-Fenzy M; Elchardus JF; Brami G; Digeon B; Gruson N; Adnet JJ
Genet Couns; 1994; 5(1):39-44. PubMed ID: 8031534
[TBL] [Abstract][Full Text] [Related]
58. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
[TBL] [Abstract][Full Text] [Related]
59. Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.
Riegel M; Hargreaves P; Baumer A; Guc-Scekic M; Ignjatovic M; Schinzel A
Eur J Med Genet; 2005; 48(2):167-74. PubMed ID: 16053908
[TBL] [Abstract][Full Text] [Related]
60. [Monosomy 7qter (author's transl)].
Lambert JC; Mariani R; Donzeau M; Ferrari M; Boutte P; Ayraud N
Arch Fr Pediatr; 1981 Mar; 38(3):177-80. PubMed ID: 7235841
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]