256 related articles for article (PubMed ID: 2290435)
1. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
Bode H; Bühler EM; Wyler F; Hadzilselimovic F
Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
[TBL] [Abstract][Full Text] [Related]
2. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
3. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Case of partial trisomy 4p+ in a child as a result of a balanced translocation in the father].
Patiutko RS; Kulieva LM; Egolina NA
Genetika; 1978 Sep; 14(9):1653-7. PubMed ID: 720831
[TBL] [Abstract][Full Text] [Related]
6. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[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. Trisomy 20p due to a paternal reciprocal translocation.
Funderburk SJ; Sparkes RS; Sparkes MC
Ann Genet; 1983; 26(2):94-7. PubMed ID: 6604493
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 7q in two siblings.
Klasen M; Schmid M; Hansmann I; Grimm T
Ann Genet; 1983; 26(2):100-2. PubMed ID: 6604481
[TBL] [Abstract][Full Text] [Related]
10. Language abnormalities and minimal physical anomalies in a boy with partial trisomy of chromosome 15.
Moedjono SJ; Needleman R; Funderburk SJ
Am J Ment Defic; 1983 May; 87(6):659-63. PubMed ID: 6869425
[No Abstract] [Full Text] [Related]
11. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
Liehr T; Heller A; Eichhorn KH; Beensen V; Schulze E; Starke H; Claussen U; Schreyer I
Prenat Diagn; 2004 Dec; 24(12):1022-4. PubMed ID: 15614895
[No Abstract] [Full Text] [Related]
15. A translocation between chromosome 1 and 10 in a boy with mental retardation and dysmorphic features.
Gambhir PS; Gole LA; Tembe MV; Saraph AA; Phadke MA; Khedkar VA
Indian Pediatr; 1991 Mar; 28(3):289-91. PubMed ID: 1937707
[No Abstract] [Full Text] [Related]
16. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
Chitayat D; Fagerstrom CL; Kalousek DK; Rootman J; Taylor GP; Hall JG
Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
[TBL] [Abstract][Full Text] [Related]
17. Familial trisomy 20p five cases and two carriers in three generations a review.
Centerwall W; Francke U
Ann Genet; 1977 Jun; 20(2):77-83. PubMed ID: 302689
[TBL] [Abstract][Full Text] [Related]
18. The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter).
Petit P; Moerman P; Fryns JP
Genet Couns; 1991; 2(3):163-5. PubMed ID: 1801853
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
Fryns JP; Kleczkowska A; Van Den Berghe H
Genet Couns; 1990; 1(2):173-7. PubMed ID: 2081001
[No Abstract] [Full Text] [Related]
[Next] [New Search]