45 related articles for article (PubMed ID: 23322595)
1. Pure Interstitial Trisomy 11q Arising from a Nonrecurrent 11q13.1q22.3 Mosaic Intrachromosomal Duplication in a Patient with Craniofacial Dysmorphism and Genital Anomalies.
Martínez Anaya D; Juárez-Velázquez MDR; Reyes Ruvalcaba S; Navarrete-Meneses MDP; Salas Labadía C; Lieberman Hernández E; Pérez-Vera P
Mol Syndromol; 2023 Aug; 14(4):310-321. PubMed ID: 37766825
[TBL] [Abstract][Full Text] [Related]
2. A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism.
Nirupam N; Maheshwari A; Gupta S; Aneja S; Seth A
J Pediatr Endocrinol Metab; 2013; 26(5-6):565-7. PubMed ID: 23412856
[TBL] [Abstract][Full Text] [Related]
3. A case of dup(3q) syndrome.
Koç A; Ekmekci AY; Ozer O
Genet Couns; 2013; 24(4):381-5. PubMed ID: 24551980
[TBL] [Abstract][Full Text] [Related]
4. Genome-Wide Array Analysis Reveals Novel Genomic Regions and Candidate Gene for Intellectual Disability.
Chen X; Li H; Chen C; Zhou L; Xu X; Xiang Y; Tang S
Mol Diagn Ther; 2018 Dec; 22(6):749-757. PubMed ID: 30259421
[TBL] [Abstract][Full Text] [Related]
5. A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.
Coelho Molck M; Simioni M; Paiva Vieira T; Paoli Monteiro F; Gil-da-Silva-Lopes VL
Mol Syndromol; 2018 Jul; 9(4):197-204. PubMed ID: 30140197
[TBL] [Abstract][Full Text] [Related]
6. A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the
Peterson JF; Basel DG; Bick DP; Chirempes B; Lorier RB; Zemlicka N; Grignon JW; Weik L; Kappes U
J Pediatr Genet; 2018 Mar; 7(1):23-28. PubMed ID: 29441218
[TBL] [Abstract][Full Text] [Related]
7. Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.
Abreu-González M; García-Delgado C; Cervantes A; Aparicio-Onofre A; Guevara-Yáñez R; Sánchez-Urbina R; Gallegos-Arreola MP; Luna-Angulo A; Estrada FJ; Morán-Barroso VF
Case Rep Genet; 2013; 2013():895259. PubMed ID: 24151567
[TBL] [Abstract][Full Text] [Related]
8. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Chern SR; Chen WM; Lee CC; Hsieh LJ; Wang W
Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
[TBL] [Abstract][Full Text] [Related]
9. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
Riegel M; Schinzel A
Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
[TBL] [Abstract][Full Text] [Related]
10. A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.
Zhu H; Hu Y; Zhu R; Yang Y; Zhu X; Wang W
Am J Med Genet A; 2013 Feb; 161A(2):327-30. PubMed ID: 23322595
[TBL] [Abstract][Full Text] [Related]
11. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
[TBL] [Abstract][Full Text] [Related]
12. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.
Rodríguez L; Bhatt SS; García-Castro M; Plasencia A; Fernández-Toral J; Abarca E; de Bello Cioffi M; Liehr T
Gene; 2014 Feb; 535(2):165-9. PubMed ID: 24316129
[TBL] [Abstract][Full Text] [Related]
13. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
Frankova YE; Holenova H; Braulke I
Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
[TBL] [Abstract][Full Text] [Related]
14. New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.
Serra G; Antona V; Cimador M; Collodoro G; Guida M; Piro E; Schierz IAM; Verde V; Giuffrè M; Corsello G
Ital J Pediatr; 2023 Feb; 49(1):17. PubMed ID: 36759911
[TBL] [Abstract][Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No 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]
