455 related articles for article (PubMed ID: 18564498)
21. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature.
Lukusa T; Vermeesch JR; Fryns JP
Genet Couns; 2005; 16(1):1-15. PubMed ID: 15844773
[TBL] [Abstract][Full Text] [Related]
24. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
[TBL] [Abstract][Full Text] [Related]
25. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
[TBL] [Abstract][Full Text] [Related]
26. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
27. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.
Courtens W; Speleman F; Messiaen L; Bormans J; Van Roy N; Vamos E
Am J Med Genet; 1997 Sep; 71(4):479-85. PubMed ID: 9286460
[TBL] [Abstract][Full Text] [Related]
28. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
29. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
30. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
Mizugishi K; Yamanaka K; Kuwajima K; Kondo I
J Hum Genet; 1998; 43(3):178-81. PubMed ID: 9747030
[TBL] [Abstract][Full Text] [Related]
31. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
32. A new case of pure partial 7q duplication.
Alfonsi M; Palka C; Morizio E; Gatta V; Franchi S; Guanciali Franchi P; Zori R; Calabrese G; Palka G; Chiarelli F
Cytogenet Genome Res; 2012; 136(1):1-5. PubMed ID: 22086126
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
35. A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures.
Busche A; Klopocki E; Ullmann R; Mundlos S; Horn D
Eur J Med Genet; 2008; 51(6):615-21. PubMed ID: 18674647
[TBL] [Abstract][Full Text] [Related]
36. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
[TBL] [Abstract][Full Text] [Related]
37. Partial trisomy of 7q: case report and literature review.
Scelsa B; Bedeschi FM; Guerneri S; Lalatta F; Introvini P
J Child Neurol; 2008 May; 23(5):572-9. PubMed ID: 18056692
[TBL] [Abstract][Full Text] [Related]
38. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
39. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
40. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
