37 related articles for article (PubMed ID: 10602115)
1. Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.
Christ LA; Crowe CA; Micale MA; Conroy JM; Schwartz S
Am J Hum Genet; 1999 Nov; 65(5):1387-95. PubMed ID: 10521304
[TBL] [Abstract][Full Text] [Related]
2. From karyotypes to precision genomics in 9p deletion and duplication syndromes.
Sams EI; Ng JK; Tate V; Claire Hou YC; Cao Y; Antonacci-Fulton L; Belhassan K; Neidich J; Mitra RD; Cole FS; Dickson P; Milbrandt J; Turner TN
HGG Adv; 2022 Jan; 3(1):100081. PubMed ID: 35047865
[TBL] [Abstract][Full Text] [Related]
3. Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome.
Miyake N; Abdel-Salam G; Yamagata T; Eid MM; Osaka H; Okamoto N; Mohamed AM; Ikeda T; Afifi HH; Piard J; van Maldergem L; Mizuguchi T; Miyatake S; Tsurusaki Y; Matsumoto N
Am J Med Genet A; 2016 Oct; 170(10):2662-70. PubMed ID: 27264538
[TBL] [Abstract][Full Text] [Related]
4. Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
Strehle EM; Yu L; Rosenfeld JA; Donkervoort S; Zhou Y; Chen TJ; Martinez JE; Fan YS; Barbouth D; Zhu H; Vaglio A; Smith R; Stevens CA; Curry CJ; Ladda RL; Fan ZJ; Fox JE; Martin JA; Abdel-Hamid HZ; McCracken EA; McGillivray BC; Masser-Frye D; Huang T
Am J Med Genet A; 2012 Sep; 158A(9):2139-51. PubMed ID: 22847869
[TBL] [Abstract][Full Text] [Related]
5. Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci.
Ledig S; Hiort O; Scherer G; Hoffmann M; Wolff G; Morlot S; Kuechler A; Wieacker P
Hum Reprod; 2010 Oct; 25(10):2637-46. PubMed ID: 20685758
[TBL] [Abstract][Full Text] [Related]
6. Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2.
Dathe K; Kjaer KW; Brehm A; Meinecke P; Nürnberg P; Neto JC; Brunoni D; Tommerup N; Ott CE; Klopocki E; Seemann P; Mundlos S
Am J Hum Genet; 2009 Apr; 84(4):483-92. PubMed ID: 19327734
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. A rare familial rearrangement of chromosomes 9 and 15 associated with intellectual disability: a clinical and molecular study.
Lemskaya NA; Romanenko SA; Rezakova MA; Filimonova EA; Prokopov DY; Dolskiy AA; Perelman PL; Maksimova YV; Shorina AR; Yudkin DV
Mol Cytogenet; 2021 Oct; 14(1):47. PubMed ID: 34607577
[TBL] [Abstract][Full Text] [Related]
9. De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation.
Leone PE; Pérez-Villa A; Yumiceba V; Hernández MÁ; García-Cárdenas JM; Armendáriz-Castillo I; Guerrero S; Guevara-Ramírez P; López-Cortés A; Zambrano AK; García JL; Hernández JM; Paz-Y-Miño C
J Pediatr Genet; 2020 Mar; 9(1):69-75. PubMed ID: 31976149
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. FISH analysis in detecting 9p duplication (p22p24).
Guanciali Franchi P; Calabrese G; Morizio E; Modestini E; Stuppia L; Mingarelli R; Palka G
Am J Med Genet; 2000 Jan; 90(1):35-7. PubMed ID: 10602115
[TBL] [Abstract][Full Text] [Related]
13. Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
Fujimoto A; Lin MS; Schwartz S
Am J Med Genet; 1998 May; 77(4):268-71. PubMed ID: 9600733
[TBL] [Abstract][Full Text] [Related]
14. 20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 Mb.
Bonaglia MC; Giorda R; Carrozzo R; Roncoroni ME; Grasso R; Borgatti R; Zuffardi O
Am J Med Genet; 2002 Oct; 112(2):154-9. PubMed ID: 12244548
[TBL] [Abstract][Full Text] [Related]
15. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
[TBL] [Abstract][Full Text] [Related]
16. Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
Mégarbané A; Gosset P; Souraty N; Lapierre JM; Korban R; Zahed L; Samaras L; Vekemans M; Prieur M
Am J Med Genet; 2001 Dec; 104(3):204-8. PubMed ID: 11754045
[TBL] [Abstract][Full Text] [Related]
17. [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]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]