247 related articles for article (PubMed ID: 12558111)
1. Partial proximal trisomy 10q syndrome: a new case.
Nucaro A; Faedda A; Cao A; Boccone L
Genet Couns; 2002; 13(4):411-6. PubMed ID: 12558111
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Trisomy 6q syndrome: a case with a << de novo >> 6q23 tandem duplication.
Causio F; Fischetto R; Carnevale F; Pansini A; Rocchi M
Genet Couns; 2001; 12(2):145-50. PubMed ID: 11491309
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
Bregant L; Gersak K; Veble A
Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
[TBL] [Abstract][Full Text] [Related]
11. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
14. Pure partial trisomy 7q: two new patients and review.
Rodríguez L; López F; Paisán L; de la Red Mdel M; Ruiz AM; Blanco M; Antelo Cortizas J; Martínez-Frías ML
Am J Med Genet; 2002 Nov; 113(2):218-24. PubMed ID: 12407716
[TBL] [Abstract][Full Text] [Related]
15. FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.
Chu TW; Teebi AS; Gibson L; Breg WR; Yang-Feng TL
Am J Med Genet; 1994 Aug; 52(1):92-6. PubMed ID: 7977471
[TBL] [Abstract][Full Text] [Related]
16. [Partial "de novo" trisomy 10q (author's transl)].
Berger R; Derre J; Murawsky M; Amiel-Tison C
J Genet Hum; 1976 Dec; 24(4):261-9. PubMed ID: 1022850
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
Hou JW
J Formos Med Assoc; 2003 Dec; 102(12):887-92. PubMed ID: 14976570
[TBL] [Abstract][Full Text] [Related]
20. Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
Starke H; Mrasek K; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):359-60. PubMed ID: 15750019
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
