160 related articles for article (PubMed ID: 23480358)
1. Patient with terminal 9 Mb deletion of chromosome 9p: refining the critical region for 9p monosomy syndrome with trigonocephaly.
Mitsui N; Shimizu K; Nishimoto H; Mochizuki H; Iida M; Ohashi H
Congenit Anom (Kyoto); 2013 Mar; 53(1):49-53. PubMed ID: 23480358
[TBL] [Abstract][Full Text] [Related]
2. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
Mohamed AM; Kamel AK; Eid MM; Eid OM; Mekkawy M; Hussein SH; Zaki MS; Esmail S; Afifi HH; El-Kamah GY; Otaify GA; El-Awady HA; Elaidy A; Essa MY; El-Ruby M; Ashaat EA; Hammad SA; Mazen I; Abdel-Salam GMH; Aglan M; Temtamy S
Mol Genet Genomic Med; 2021 Nov; 9(11):e1829. PubMed ID: 34609792
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23.
Kawara H; Yamamoto T; Harada N; Yoshiura K; Niikawa N; Nishimura A; Mizuguchi T; Matsumoto N
Am J Med Genet A; 2006 Feb; 140(4):373-7. PubMed ID: 16419130
[TBL] [Abstract][Full Text] [Related]
6. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
[TBL] [Abstract][Full Text] [Related]
7. Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p.
Hauge X; Raca G; Cooper S; May K; Spiro R; Adam M; Martin CL
Genet Med; 2008 Aug; 10(8):599-611. PubMed ID: 18641517
[TBL] [Abstract][Full Text] [Related]
8. 9p partial monosomy and disorders of sex development: review and postulation of a pathogenetic mechanism.
Quinonez SC; Park JM; Rabah R; Owens KM; Yashar BM; Glover TW; Keegan CE
Am J Med Genet A; 2013 Aug; 161A(8):1882-96. PubMed ID: 23824832
[TBL] [Abstract][Full Text] [Related]
9. Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.
Swinkels ME; Simons A; Smeets DF; Vissers LE; Veltman JA; Pfundt R; de Vries BB; Faas BH; Schrander-Stumpel CT; McCann E; Sweeney E; May P; Draaisma JM; Knoers NV; van Kessel AG; van Ravenswaaij-Arts CM
Am J Med Genet A; 2008 Jun; 146A(11):1430-8. PubMed ID: 18452192
[TBL] [Abstract][Full Text] [Related]
10. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
[TBL] [Abstract][Full Text] [Related]
11. Short clinical report: a new case with de novo partial 9p monosomy.
Nagy E; Bod M; Nemeth I; Timar L
Acta Paediatr Hung; 1991; 31(4):407-13. PubMed ID: 1790023
[TBL] [Abstract][Full Text] [Related]
12. FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.
Shan Z; Zabel B; Trautmann U; Hillig U; Ottolenghi C; Wan Y; Haaf T
Eur J Hum Genet; 2000 Mar; 8(3):167-73. PubMed ID: 10780781
[TBL] [Abstract][Full Text] [Related]
13. Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions.
Onesimo R; Orteschi D; Scalzone M; Rossodivita A; Nanni L; Zannoni GF; Marrocco G; Battaglia D; Fundarò C; Neri G
Am J Med Genet A; 2012 Sep; 158A(9):2266-71. PubMed ID: 22821627
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.
Yang Y; Wang C; Wang F; Zhu L; Liu H; He X
Gene; 2012 Jul; 502(2):154-8. PubMed ID: 22555022
[TBL] [Abstract][Full Text] [Related]
16. Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.
Hoo JJ; Fischer A; Fuhrmann W
Ann Genet; 1982; 25(4):249-52. PubMed ID: 6985017
[TBL] [Abstract][Full Text] [Related]
17. Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis.
Hou QF; Wu D; Chu Y; Liao SX
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):867-870. PubMed ID: 28040136
[TBL] [Abstract][Full Text] [Related]
18. Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1.
Veitia R; Nunes M; Brauner R; Doco-Fenzy M; Joanny-Flinois O; Jaubert F; Lortat-Jacob S; Fellous M; McElreavey K
Genomics; 1997 Apr; 41(2):271-4. PubMed ID: 9143505
[TBL] [Abstract][Full Text] [Related]
19. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
[TBL] [Abstract][Full Text] [Related]
20. Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.
Ounap K; Uibo O; Zordania R; Kiho L; Ilus T; Oiglane-Shlik E; Bartsch O
Am J Med Genet A; 2004 Nov; 130A(4):415-23. PubMed ID: 15481033
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
