152 related articles for article (PubMed ID: 20681221)
1. Two cases with partial trisomy 9: cytogenetic and clinical findings.
Ozer O; Derbent M; Sahin FI; Yilmaz Z
Genet Couns; 2010; 21(2):205-13. PubMed ID: 20681221
[TBL] [Abstract][Full Text] [Related]
2. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
3. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
[TBL] [Abstract][Full Text] [Related]
4. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
5. The phenotypic and cytogenetic spectrum of partial trisomy 9.
Wilson GN; Raj A; Baker D
Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
[TBL] [Abstract][Full Text] [Related]
6. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
[TBL] [Abstract][Full Text] [Related]
7. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
[TBL] [Abstract][Full Text] [Related]
8. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations.
Crane J; Sujansky E; Smith A
Am J Med Genet; 1979; 4(3):219-29. PubMed ID: 517577
[TBL] [Abstract][Full Text] [Related]
11. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
Zankl M; Schwanitz G; Schmid P; Zankl H; Dockter G; Rodewald A; Zang KD; Grosse KP
Am J Med Genet; 1979; 4(1):5-16. PubMed ID: 495653
[TBL] [Abstract][Full Text] [Related]
12. Distal partial trisomy 1q: report of two cases and a review of the literature.
Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
Hacihanefioğlu S; Güven GS; Deviren A; Silahtaroğlu AN; Yosunvkaya Fenerci E; Ozkiliç A; Yüksel A
Genet Couns; 2002; 13(1):41-8. PubMed ID: 12017237
[TBL] [Abstract][Full Text] [Related]
16. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
[TBL] [Abstract][Full Text] [Related]
19. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic and molecular analysis in trisomy 12p.
Allen TL; Brothman AR; Carey JC; Chance PF
Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]