143 related articles for article (PubMed ID: 1536172)
1. Duplication of distal 19q: clinical report and review.
Boyd E; Grass FS; Parke JC; Knutson K; Stevenson RE
Am J Med Genet; 1992 Feb; 42(3):326-30. PubMed ID: 1536172
[TBL] [Abstract][Full Text] [Related]
2. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
Sparkes RS; Francke U; Muller H; Toomey K
Ann Genet; 1977 Mar; 20(1):31-5. PubMed ID: 302670
[TBL] [Abstract][Full Text] [Related]
3. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
Legare JM; Sekhon GS; Laxova R
Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
[TBL] [Abstract][Full Text] [Related]
4. [11q distal trisomy due to a familial 11;18 translocation].
Menéndez I; Rivera H; Morales E; Juan J; Jiménez M
Bol Med Hosp Infant Mex; 1990 Nov; 47(11):792-4. PubMed ID: 2285470
[TBL] [Abstract][Full Text] [Related]
5. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
[TBL] [Abstract][Full Text] [Related]
6. [Proximal monosomy 13].
Geormăneanu M; Geormăneanu C
Ann Genet; 1990; 33(3):176-8. PubMed ID: 2288464
[TBL] [Abstract][Full Text] [Related]
7. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
8. Duplication of distal 22q.
Abeliovich D; Maor E; Bashan N; Carmi R
Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
[TBL] [Abstract][Full Text] [Related]
9. Partial duplication of distal 17q.
Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
[TBL] [Abstract][Full Text] [Related]
10. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
11. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
Odell JM; Siebert JR; Bradley C; Salk D
Am J Med Genet; 1987 Jul; 27(3):687-92. PubMed ID: 3631140
[TBL] [Abstract][Full Text] [Related]
12. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Duplication 7p de novo and literature review.
Zerres K; Schwanitz G; Gellissen K; Schroers L; Sohler R
Ann Genet; 1989; 32(4):225-9. PubMed ID: 2692511
[TBL] [Abstract][Full Text] [Related]
15. 19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocation.
Rivas F; García-Cruz D; Rivera H; Plascencia ML; González RM; Cantú JM
Ann Genet; 1985; 28(2):113-5. PubMed ID: 3876059
[TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
[No Abstract] [Full Text] [Related]
17. Ring chromosome 22 and autism: report and review.
MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
[TBL] [Abstract][Full Text] [Related]
18. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
[TBL] [Abstract][Full Text] [Related]
19. Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.
Vraneković J; Brajenović-Milić B; Modrusan-Mozetić Z; Babić I; Kapović M
Cytogenet Genome Res; 2008; 121(3-4):298-301. PubMed ID: 18758176
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 16p in a liveborn infant and review of trisomy 16p.
O'Connor TA; Higgins RR
Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
