101 related articles for article (PubMed ID: 1296518)
1. Trisomy of the short arm of chromosome 4: the changing phenotype with age.
Kleczkowska A; Fryns JP; van den Berghe H
Ann Genet; 1992; 35(4):217-23. PubMed ID: 1296518
[TBL] [Abstract][Full Text] [Related]
2. Trisomy of the distal third of the long arm of chromosome 10. Report of a new case due to a familial translocation t(10;18) (q24;p11).
Forabosco A; Bernasconi S; Giovannelli G; Dutrillaux B
Helv Paediatr Acta; 1975 Oct; 30(3):289-95. PubMed ID: 1184398
[TBL] [Abstract][Full Text] [Related]
3. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
Coco R; Penchaszadeh VB
J Genet Hum; 1978 Sep; 26(3):203-10. PubMed ID: 739260
[TBL] [Abstract][Full Text] [Related]
4. The trisomy 4p syndrome: case report and review.
Gonzalez CH; Sommer A; Meisner LF; Elejalde BR; Opitz JM
Am J Med Genet; 1977; 1(2):137-56. PubMed ID: 416713
[TBL] [Abstract][Full Text] [Related]
5. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
[TBL] [Abstract][Full Text] [Related]
6. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
[TBL] [Abstract][Full Text] [Related]
7. [Cp trisomy: a new syndrome].
Canu JM; Buentello L; Armendares S
Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
[No Abstract] [Full Text] [Related]
8. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 5: delineation of clinical features.
DiLiberti JH; McKean R; Webb MJ; Williams G
Birth Defects Orig Artic Ser; 1977; 13(3C):185-94. PubMed ID: 890110
[TBL] [Abstract][Full Text] [Related]
10. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
Frankova YE; Holenova H; Braulke I
Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
[TBL] [Abstract][Full Text] [Related]
11. Natural history of mosaic trisomy 14 syndrome.
Fujimoto A; Allanson J; Crowe CA; Lipson MH; Johnson VP
Am J Med Genet; 1992 Sep; 44(2):189-96. PubMed ID: 1456290
[TBL] [Abstract][Full Text] [Related]
12. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
Brooks SS; Wisniewski K; Brown WT
Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
[TBL] [Abstract][Full Text] [Related]
13. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
Tschernigg M; Petek E; Wagner K; Kroisel PM
Genet Couns; 2002; 13(1):29-33. PubMed ID: 12017235
[TBL] [Abstract][Full Text] [Related]
14. The 18p- syndrome. Report of five cases.
Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
[TBL] [Abstract][Full Text] [Related]
15. Partial trisomy of chromosome 14: (+14q-).
Yeatman GW; Riccardi VM
Birth Defects Orig Artic Ser; 1976; 12(5):119-24. PubMed ID: 953211
[TBL] [Abstract][Full Text] [Related]
16. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
17. [Deletion of the short arm of chromosome 18 and trisomy 18 in a pair of siblings with unusual form of porphyria].
Simon N; Hunyadi J; Szörényi A; Szemere G
Hautarzt; 1973 May; 24(5):185-9. PubMed ID: 4753369
[No Abstract] [Full Text] [Related]
18. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
[TBL] [Abstract][Full Text] [Related]
19. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
20. [Trisomy 10q24--10qter].
Dutrillaux B; Laurent C; Bernasconi S; Lejeune J
Ann Genet; 1975 Dec; 18(4):217-22. PubMed ID: 1083188
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]