429 related articles for article (PubMed ID: 17710874)
1. 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]
2. [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]
3. 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]
4. 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]
5. [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]
6. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
Saad A; Khelif M; Kharrat H; Bouzakoura C
Ann Pediatr (Paris); 1991 May; 38(5):350-4. PubMed ID: 1872531
[TBL] [Abstract][Full Text] [Related]
7. High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement.
Qumsiyeh MB; Wilroy RS; Peeden JN; Tharapel AT
Am J Med Genet; 1991 Oct; 41(1):99-101. PubMed ID: 1719815
[TBL] [Abstract][Full Text] [Related]
8. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC
Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
[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. 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]
11. [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].
Raoul O; Carpentier S; Dutrillaux B; Mallet R; Lejeune J
Ann Genet; 1976 Sep; 19(3):187-90. PubMed ID: 136225
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. [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]
15. Partial trisomy 13q22----qter. A new case.
Galán F; García R; Aguilar MS; Moya M
Ann Genet; 1989; 32(2):114-6. PubMed ID: 2757360
[TBL] [Abstract][Full Text] [Related]
16. The 12p trisomy syndrome.
Armendares S; Salamanca F; Nava S; Ramirez S; Cantu JM
Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
[TBL] [Abstract][Full Text] [Related]
17. Partial duplication of 17 long arm.
Lenzini E; Leszl A; Artifoni L; Casellato R; Tenconi R; Baccichetti C
Ann Genet; 1988; 31(3):175-80. PubMed ID: 3265610
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
Mewar R; Kline AD; Jackson L; Overhauser J
Am J Med Genet; 1992 Nov; 44(4):477-81. PubMed ID: 1442891
[TBL] [Abstract][Full Text] [Related]
20. Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.
Williams CA; Frias JL; McCormick MK; Antonarakis SE; Cantu ES
Am J Med Genet Suppl; 1990; 7():110-4. PubMed ID: 2149936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
