102 related articles for article (PubMed ID: 7258223)
1. Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1 leads to q24 in different offspring.
Williamson RA; Donlan MA; Dolan CR; Thuline HC; Harrison MT; Hall JG
Am J Med Genet; 1981; 9(2):105-11. PubMed ID: 7258223
[TBL] [Abstract][Full Text] [Related]
2. Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father.
Pai GS; Rogers JF; Sommer A
Am J Med Genet; 1983 Jan; 14(1):189-95. PubMed ID: 6829607
[TBL] [Abstract][Full Text] [Related]
3. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 leads to 7p21.
Miller M; Kaufman G; Reed G; Bilenker R; Schinzel A
Am J Med Genet; 1979; 4(4):323-32. PubMed ID: 539602
[TBL] [Abstract][Full Text] [Related]
4. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two families.
Liberfarb RM; Breg WR; Atkins L; Holmes LB
Am J Med Genet; 1979; 4(1):27-37. PubMed ID: 495650
[TBL] [Abstract][Full Text] [Related]
5. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
[TBL] [Abstract][Full Text] [Related]
6. Malformation syndrome of duplication 12q24.1 leads to qter.
Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
[TBL] [Abstract][Full Text] [Related]
7. Duplication (12q) syndrome in female cousins, resulting from maternal (11;12) (p15.5;q24.2) translocations.
McCorquodale MM; Rolf J; Ruppert ES; Kurczynski TW; Kolacki P
Am J Med Genet; 1986 Aug; 24(4):613-22. PubMed ID: 3740096
[TBL] [Abstract][Full Text] [Related]
8. Unbalanced translocation (3;5)(q26.1;p14): a clinical report.
Rossi M; Di Micco P; Perone L; De Brasi D; Guzzetta V; Andreucci MV; Vega GR; Marzano MG; Iaccarino E; Andria G
Am J Med Genet; 2002 Jul; 110(4):353-8. PubMed ID: 12116209
[TBL] [Abstract][Full Text] [Related]
9. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM
Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399
[TBL] [Abstract][Full Text] [Related]
10. Resolution of breakpoints in a complex rearrangement by use of multiple staining techniques: confirmation of suspected 12p12.3 intraband by deletion dosage effect of LDHB.
Magenis E; Brown MG; Chamberlin J; Donlon T; Hepburn D; Lamvik N; Lovrien E; Yoshitomi M
Am J Med Genet; 1981; 9(2):95-103. PubMed ID: 6167167
[TBL] [Abstract][Full Text] [Related]
11. Mental retardation/shortness of stature/multiple minor anomalies syndrome associated with insertion of 3q material into 18p.
al-Attia HM; Sedaghatian MR
Am J Med Genet; 1995 Mar; 56(1):35-8. PubMed ID: 7747783
[TBL] [Abstract][Full Text] [Related]
12. Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation.
Shaffer LG; Hecht JT; Ledbetter DH; Greenberg F
Am J Med Genet; 1993 Mar; 45(5):581-3. PubMed ID: 8456828
[TBL] [Abstract][Full Text] [Related]
13. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
Wheeler PG; Weaver DD; Palmer CG
Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
[TBL] [Abstract][Full Text] [Related]
14. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.
Cohen MM; Lerner C; Balkin NE
Am J Med Genet; 1983 Jan; 14(1):89-96. PubMed ID: 6829613
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Multiple congenital anomalies in a man with (X;6) translocation.
Sivak LE; Esbenshade J; Brothman AR; Issa B; Lemons RS; Carey JC
Am J Med Genet; 1994 May; 51(1):9-12. PubMed ID: 8030680
[TBL] [Abstract][Full Text] [Related]
17. Monosomy 11q: report of two familial cases and review of the literature.
Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
[TBL] [Abstract][Full Text] [Related]
18. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
19. 2q35qter duplication syndrome: phenotypic definition.
Grammatico P; Di Rosa C; Rinaldi R; Roccella M; Cupilari F; Sbezzi T; Del Porto G
Genet Couns; 1997; 8(4):327-34. PubMed ID: 9457503
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]