253 related articles for article (PubMed ID: 8055322)
21. Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases.
Crété N; Gosset P; Théophile D; Duterque-Coquillaud M; Blouin JL; Vayssettes C; Sinet PM; Créau-Goldberg N
Eur J Hum Genet; 1993; 1(1):51-63. PubMed ID: 8069651
[TBL] [Abstract][Full Text] [Related]
22. A Down syndrome female infant with partial trisomy of chromosome 21--abnormal nuchal translucency screening test.
Strah D; Veble A; Rudolf G; Writzl K; Gersak K
Genet Couns; 2008; 19(4):429-32. PubMed ID: 19239088
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Partial trisomy of chromosome 21 without the Down syndrome phenotype.
Su MT; Kuan LC; Chou YY; Tan SY; Kuo TC; Kuo PL
Prenat Diagn; 2016 May; 36(5):492-5. PubMed ID: 26918398
[No Abstract] [Full Text] [Related]
25. Clinical, cytogenetic, and molecular genetic characterization of two unrelated patients with different duplications of 21q.
Petersen MB; Tranebjaerg L; McCormick MK; Michelsen N; Mikkelsen M; Antonarakis SE
Am J Med Genet Suppl; 1990; 7():104-9. PubMed ID: 2149934
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. An extra idic(21)(q22.1) in a child with some features of Down's syndrome.
Gütiérrez-Angulo M; Ramos AL; Dávalos N; Sánchez-Corona J; Rivera H
Clin Genet; 1999 Mar; 55(3):203-6. PubMed ID: 10334475
[TBL] [Abstract][Full Text] [Related]
29. A girl with Down syndrome and partial trisomy for 21pter-q22.13: a clue to narrow the Down syndrome critical region.
Sato D; Kawara H; Shimokawa O; Harada N; Tonoki H; Takahashi N; Imai Y; Kimura H; Matsumoto N; Ariga T; Niikawa N; Yoshiura K
Am J Med Genet A; 2008 Jan; 146A(1):124-7. PubMed ID: 18074380
[No Abstract] [Full Text] [Related]
30. A patient with Down syndrome with a de novo derivative chromosome 21.
Cetin Z; Yakut S; Mihci E; Manguoglu AE; Berker S; Keser I; Luleci G
Gene; 2012 Oct; 507(2):159-64. PubMed ID: 22827956
[TBL] [Abstract][Full Text] [Related]
31. A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart.
Fuentes JJ; Pritchard MA; Planas AM; Bosch A; Ferrer I; Estivill X
Hum Mol Genet; 1995 Oct; 4(10):1935-44. PubMed ID: 8595418
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. A high-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2.
Gosset P; Crété N; Ait Ghezala G; Théophile D; Van Broeckhoven C; Vayssettes C; Sinet PM; Créau N
Mamm Genome; 1995 Feb; 6(2):127-30. PubMed ID: 7766996
[No Abstract] [Full Text] [Related]
34. High-resolution physical map and identification of potentially regulatory sequences of the human SH3BGR located in the Down syndrome chromosomal region.
Vidal-Taboada JM; Bergoñon S; Scartezzini P; Egeo A; Nizetic D; Oliva R
Biochem Biophys Res Commun; 1997 Dec; 241(2):321-6. PubMed ID: 9425270
[TBL] [Abstract][Full Text] [Related]
35. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
[TBL] [Abstract][Full Text] [Related]
36. Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.
Muenke M; Bone LJ; Mitchell HF; Hart I; Walton K; Hall-Johnson K; Ippel EF; Dietz-Band J; Kvaløy K; Fan CM
Am J Hum Genet; 1995 Nov; 57(5):1074-9. PubMed ID: 7485157
[TBL] [Abstract][Full Text] [Related]
37. Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessment.
Barnicoat AJ; Bonneau JL; Boyd E; Docherty Z; Fennell SJ; Huret JL; King M; Maltby EL; McManus S; Pilz DT; Shafei-Benaissa E; Super M; Tolmie J
Clin Genet; 1996 Jan; 49(1):20-7. PubMed ID: 8721567
[TBL] [Abstract][Full Text] [Related]
38. A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype.
Papoulidis I; Papageorgiou E; Siomou E; Oikonomidou E; Thomaidis L; Vetro A; Zuffardi O; Liehr T; Manolakos E; Vassilis P
Gene; 2014 Feb; 536(2):441-3. PubMed ID: 24334122
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.
Dahmane N; Ghezala GA; Gosset P; Chamoun Z; Dufresne-Zacharia MC; Lopes C; Rabatel N; Gassanova-Maugenre S; Chettouh Z; Abramowski V; Fayet E; Yaspo ML; Korn B; Blouin JL; Lehrach H; Poutska A; Antonarakis SE; Sinet PM; Créau N; Delabar JM
Genomics; 1998 Feb; 48(1):12-23. PubMed ID: 9503011
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]