169 related articles for article (PubMed ID: 21948691)
21. Duplication 9p and their implication to phenotype.
Guilherme RS; Meloni VA; Perez AB; Pilla AL; de Ramos MA; Dantas AG; Takeno SS; Kulikowski LD; Melaragno MI
BMC Med Genet; 2014 Dec; 15():142. PubMed ID: 25526829
[TBL] [Abstract][Full Text] [Related]
22. Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report.
Li R; Wang C; Zhang Z; Li D; Li L; Zhao D; Xu Z
BMC Pediatr; 2023 Apr; 23(1):168. PubMed ID: 37046298
[TBL] [Abstract][Full Text] [Related]
23. Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.
Velagaleti GV; Hawkins JC; Panova NI; Lockhart LH
Indian J Pediatr; 2008 Sep; 75(9):956-60. PubMed ID: 18568304
[TBL] [Abstract][Full Text] [Related]
24. Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female.
Hulick PJ; Noonan KM; Kulkarni S; Donovan DJ; Listewnik M; Ihm C; Stoler JM; Weremowicz S
Cytogenet Genome Res; 2009; 126(3):305-12. PubMed ID: 20068300
[TBL] [Abstract][Full Text] [Related]
25. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
[TBL] [Abstract][Full Text] [Related]
26. Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter.
Fukushi D; Kurosawa K; Suzuki Y; Suzuki K; Yamada K; Watanabe S; Yokochi K; Wakamatsu N
Am J Med Genet A; 2017 Aug; 173(8):2201-2209. PubMed ID: 28599099
[TBL] [Abstract][Full Text] [Related]
27. A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.
Eid MO; Eid MM; Kamel AK; El-Ruby M; Abdel-Salam GM
Genet Couns; 2015; 26(2):153-61. PubMed ID: 26349184
[TBL] [Abstract][Full Text] [Related]
28. Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter.
Gruchy N; Jacquemont ML; Lyonnet S; Labrune P; El Kamel I; Siffroi JP; Portnoï MF
Am J Med Genet A; 2007 Oct; 143A(20):2417-22. PubMed ID: 17853488
[TBL] [Abstract][Full Text] [Related]
29. Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.
Manolakos E; Vetro A; Papadopoulou E; Kefalas K; Lagou M; Thomaidis L; Peitsidis P; Sifakis S; Divane A; Ziegler M; Liehr T; Zuffardi O; Papoulidis I
Cytogenet Genome Res; 2013; 140(1):12-20. PubMed ID: 23652918
[TBL] [Abstract][Full Text] [Related]
30. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
[TBL] [Abstract][Full Text] [Related]
31. Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
Wieczorek D; Bartsch O; Gillessen-Kaesbach G
Am J Med Genet A; 2003 Jul; 120A(3):429-33. PubMed ID: 12838568
[TBL] [Abstract][Full Text] [Related]
32. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
33. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
[TBL] [Abstract][Full Text] [Related]
35. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
36. Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature.
la Cour Sibbesen E; Jespersgaard C; Alosi D; Bisgaard AM; Tümer Z
Am J Med Genet A; 2013 Jun; 161A(6):1447-52. PubMed ID: 23633410
[TBL] [Abstract][Full Text] [Related]
37. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
38. [Detection of 9p partial trisomy using array-based comparative genomic hybridization].
Zhou XY; Hu P; Yang YQ; Li L; Wang Y; Yu ZB; Han SP; Guo XR; Xu ZF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):52-5. PubMed ID: 22311492
[TBL] [Abstract][Full Text] [Related]
39. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
[TBL] [Abstract][Full Text] [Related]
40. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
Lyons MJ; Fuller JD; Montoya Mdel C; DuPont BR; Holden KR
J Child Neurol; 2013 Apr; 28(4):524-6. PubMed ID: 22752474
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
