210 related articles for article (PubMed ID: 25752286)
21. 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]
22. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
Zumkeller W; Volleth M; Muschke P; Tönnies H; Heller A; Liehr T; Wieacker P; Stumm M
Am J Med Genet A; 2004 Sep; 129A(3):261-4. PubMed ID: 15326625
[TBL] [Abstract][Full Text] [Related]
23. [Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization].
Guo C; Wang J; Zhao L; Liu J; Wang J; Xiao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):375-7. PubMed ID: 26037354
[TBL] [Abstract][Full Text] [Related]
24. Trisomy 16q21 --> qter: Seven-year follow-up of a girl with unusually long survival.
de Carvalho AF; da Silva Bellucco FT; dos Santos NP; Pellegrino R; de Azevedo Moreira LM; Toralles MB; Kulikowski LD; Melaragno MI
Am J Med Genet A; 2010 Aug; 152A(8):2074-8. PubMed ID: 20635361
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. A de novo reciprocal t(2;18) translocation with regular trisomy 21.
Cyrus C; Kaur H; Koshy T; Thankanadar J; Nallathambi C
Genet Test; 2007; 11(4):459-62. PubMed ID: 18294065
[TBL] [Abstract][Full Text] [Related]
27. Cytogenetical diagnosis in paraffin-embedded fetoplacental tissue using comparative genomic hybridization.
Ozcan T; Burki N; Parkash V; Huang X; Pejovic T; Mahoney MJ; Ward DC
Prenat Diagn; 2000 Jan; 20(1):41-4. PubMed ID: 10701850
[TBL] [Abstract][Full Text] [Related]
28. Trisomy 4q syndrome: presentation of a new case and review of the literature.
Lundin C; Zech L; Sjörs K; Wadelius C; Annerén G
Ann Genet; 2002; 45(2):53-7. PubMed ID: 12119211
[TBL] [Abstract][Full Text] [Related]
29. Large duplication 4q25-q34 with mild clinical effect.
Elghezal H; Sendi HS; Monastiri K; Lapierre JM; Romdhane SI; Mougou S; Saad A
Ann Genet; 2004; 47(4):419-22. PubMed ID: 15581841
[TBL] [Abstract][Full Text] [Related]
30. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
Akalin I; Bozdag S; Spielmann M; Basaran SY; Nanda I; Klopocki E
Am J Med Genet A; 2014 Feb; 164A(2):490-4. PubMed ID: 24311106
[TBL] [Abstract][Full Text] [Related]
31. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
32. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
[TBL] [Abstract][Full Text] [Related]
33. Pure partial trisomy 7q: two new patients and review.
Rodríguez L; López F; Paisán L; de la Red Mdel M; Ruiz AM; Blanco M; Antelo Cortizas J; Martínez-Frías ML
Am J Med Genet; 2002 Nov; 113(2):218-24. PubMed ID: 12407716
[TBL] [Abstract][Full Text] [Related]
34. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
35. Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen.
Fritz B; Greber-Platzer S; Frischer T; Streubel B; Gröblacher J; Amann G; Ventruba P; Rehder H; Fonatsch C
Am J Med Genet; 2000 Oct; 94(4):271-80. PubMed ID: 11038438
[TBL] [Abstract][Full Text] [Related]
36. 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?
Bass HN; Weber-Parisi F; Sparkes RS
J Med Genet; 1978 Oct; 15(5):391-5. PubMed ID: 739531
[TBL] [Abstract][Full Text] [Related]
37. Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement.
Tzschach A; Menzel C; Erdogan F; Istifli ES; Rieger M; Ovens-Raeder A; Macke A; Ropers HH; Ullmann R; Kalscheuer V
Am J Med Genet A; 2010 Apr; 152A(4):1008-12. PubMed ID: 20358617
[TBL] [Abstract][Full Text] [Related]
38. Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.
Nadal M; Moreno S; Pritchard M; Preciado MA; Estivill X; Ramos-Arroyo MA
J Med Genet; 1997 Jan; 34(1):50-4. PubMed ID: 9032650
[TBL] [Abstract][Full Text] [Related]
39. A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.
Assawamakin A; Wattanasirichaigoon D; Tocharoentanaphol C; Waeteekul S; Tansatit M; Thongnoppakhun W; Limwongse C
Am J Med Genet A; 2012 Apr; 158A(4):901-8. PubMed ID: 22419381
[TBL] [Abstract][Full Text] [Related]
40. Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH).
Jeziorowska A; Houck GE; Yao XL; Sklower-Brooks SL; Wisniewski KE; Jenkins EC; Wisniewski HM
Clin Genet; 1992 Sep; 42(3):124-8. PubMed ID: 1395083
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]