168 related articles for article (PubMed ID: 6448566)
1. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation.
Cantu JM; Hernandez A; Plascencia L; Vaca G; Moller M; Rivera H
Ann Genet; 1980; 23(3):183-6. PubMed ID: 6448566
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
3. [Partial trisomy for the segment 21(q11----qter) resulting from a de novo translocation between chromosomes 5 and 21].
Crippa L; Ballaman J; Engel E
Ann Genet; 1984; 27(3):190-3. PubMed ID: 6239590
[TBL] [Abstract][Full Text] [Related]
4. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
Rivera H; Rivas F; Plascencia L; Cantú JM
Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.
Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G
J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105
[TBL] [Abstract][Full Text] [Related]
7. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
8. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
9. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
[TBL] [Abstract][Full Text] [Related]
10. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
Back E; Stier R; Böhm N; Adlung A; Hameister H
Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606
[TBL] [Abstract][Full Text] [Related]
11. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW
Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619
[TBL] [Abstract][Full Text] [Related]
12. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
[TBL] [Abstract][Full Text] [Related]
13. De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis.
Reynolds JF; Wyandt HE; Kelly TE
Am J Med Genet; 1985 Jan; 20(1):173-80. PubMed ID: 3970070
[TBL] [Abstract][Full Text] [Related]
14. Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy.
Tuysuz B; Yavuz A; Ozdil M; Caferler J; Ozon H
Genet Couns; 2010; 21(1):61-7. PubMed ID: 20420031
[TBL] [Abstract][Full Text] [Related]
15. Unusual chromosome aberrations in 3 children with Down syndrome.
Osztovics M; Tóth S; Wilhelm O
Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
[TBL] [Abstract][Full Text] [Related]
16. Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomy.
Garcia-Esquivel L; Rivera H; Sanchez-Corona J; Ramirez ML; Jimenez M; Cantú JM
Ann Genet; 1987; 30(2):94-7. PubMed ID: 3499849
[TBL] [Abstract][Full Text] [Related]
17. Partial monosomy 15q due to de novo t(15;22)(q15;p11).
Mori MA; Rodriguez L; Pinel I; Casas JM; Diaz de Bustamante A; Martinez-Frias ML
Ann Genet; 1987; 30(4):246-8. PubMed ID: 3322163
[TBL] [Abstract][Full Text] [Related]
18. Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
Theodoropoulos DS; Cowan JM; Elias ER; Cole C
Am J Med Genet; 1995 Nov; 59(2):161-3. PubMed ID: 8588579
[TBL] [Abstract][Full Text] [Related]
19. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
Scott JA; Wenger SL; Steele MW; Chakravarti A
Am J Med Genet; 1995 Mar; 56(1):67-71. PubMed ID: 7747789
[TBL] [Abstract][Full Text] [Related]
20. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]