181 related articles for article (PubMed ID: 10861659)
1. Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family.
Braddock SR; Henley KM; Potter KL; Nguyen HG; Huang TH
Am J Med Genet; 2000 Jun; 92(5):311-7. PubMed ID: 10861659
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ
J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708
[TBL] [Abstract][Full Text] [Related]
5. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
[TBL] [Abstract][Full Text] [Related]
6. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
Wang XR; Luo RL; Dai XH; Liu JY
Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation.
Velinov M; Gu H; Yeboa K; Warburton D; Tubo T; Dhuper S; Lanter S; Delprino D; Kupchik G; Jenkins EC
Am J Med Genet; 2002 Feb; 107(4):330-3. PubMed ID: 11840491
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome.
Kondo Y; Mizuno S; Ohara K; Nakamura T; Yamada K; Yamamori S; Hayakawa C; Ishii T; Yamada Y; Wakamatsu N
Am J Med Genet A; 2006 Feb; 140(3):227-32. PubMed ID: 16411203
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11).
Mutchinick O; Ruz L; Jiménez R
Hum Genet; 1978 Nov; 45(1):89-95. PubMed ID: 730186
[TBL] [Abstract][Full Text] [Related]
14. Recurrent abortions and down syndrome resulting from Robertsonian translocation 21q; 21q.
Kolgeci S; Azemi M; Ahmeti H; Dervishi Z; Sopjani M; Kolgeci J
Med Arch; 2012; 66(5):350-2. PubMed ID: 23097978
[TBL] [Abstract][Full Text] [Related]
15. Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.
Horn D; Neitzel H; Tönnies H; Kalscheuer V; Kunze J; Hinkel GK; Bartsch O
Am J Med Genet A; 2003 Mar; 117A(3):236-44. PubMed ID: 12599186
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.
Bartsch O; König U; Petersen MB; Poulsen H; Mikkelsen M; Palau F; Prieto F; Schwinger E
Hum Genet; 1993 Sep; 92(2):127-32. PubMed ID: 8370577
[TBL] [Abstract][Full Text] [Related]
18. YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.
Nadal M; Milà M; Pritchard M; Mur A; Pujals J; Blouin JL; Antonarakis SE; Ballesta F; Estivill X
Hum Genet; 1996 Oct; 98(4):460-6. PubMed ID: 8792823
[TBL] [Abstract][Full Text] [Related]
19. Clinical, cytogenetic, and molecular characterization of a girl with some clinical features of Down syndrome resulting from a pure partial trisomy 21q22.11-qter due to a de novo intrachromosomal duplication.
Vaglio A; Milunsky A; Quadrelli A; Huang XL; Maher T; Mechoso B; Martínez S; Pagano S; Bellini S; Costabel M; Quadrelli R
Genet Test Mol Biomarkers; 2010 Feb; 14(1):57-65. PubMed ID: 20143912
[TBL] [Abstract][Full Text] [Related]
20. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
Balci S; Aypar E; Beksaç MS; Bartsch O
Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
