159 related articles for article (PubMed ID: 23317051)
1. 7q36 deletion and 9p22 duplication: effects of a double imbalance.
Pelegrino Kde O; Sugayama S; Catelani AL; Lezirovitz K; Kok F; Chauffaille Mde L
Mol Cytogenet; 2013 Jan; 6(1):2. PubMed ID: 23317051
[TBL] [Abstract][Full Text] [Related]
2. Simultaneous 9p Deletion and 8p Duplication in a Seven-Year-Old Girl, Detected Using Multiplex Ligation-Dependent Probe Amplification: A Case Report.
Saberi M; Mahjoub F
Iran J Med Sci; 2022 Sep; 47(5):494-499. PubMed ID: 36117579
[TBL] [Abstract][Full Text] [Related]
3. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).
Shim SH; Shim JS; Min K; Lee HS; Park JE; Park SH; Hwang E; Kim M
Gene; 2014 Jan; 534(1):100-6. PubMed ID: 24095776
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Patient With Delayed Development Resulting From
Choi A; Oh JY; Kim M; Jang W; Jang DH
Ann Rehabil Med; 2017 Oct; 41(5):881-886. PubMed ID: 29201829
[TBL] [Abstract][Full Text] [Related]
6. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
8. The use of array-CGH in a cohort of Greek children with developmental delay.
Manolakos E; Vetro A; Kefalas K; Rapti SM; Louizou E; Garas A; Kitsos G; Vasileiadis L; Tsoplou P; Eleftheriades M; Peitsidis P; Orru S; Liehr T; Petersen MB; Thomaidis L
Mol Cytogenet; 2010 Nov; 3():22. PubMed ID: 21062444
[TBL] [Abstract][Full Text] [Related]
9. Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.
Horn D; Tönnies H; Neitzel H; Wahl D; Hinkel GK; von Moers A; Bartsch O
Am J Med Genet A; 2004 Jul; 128A(1):85-92. PubMed ID: 15211664
[TBL] [Abstract][Full Text] [Related]
10. Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype.
Frühmesser A; Haberlandt E; Judmaier W; Schinzel A; Utermann B; Erdel M; Fauth C; Utermann G; Zschocke J; Kotzot D
Am J Med Genet A; 2012 Sep; 158A(9):2239-44. PubMed ID: 22821890
[TBL] [Abstract][Full Text] [Related]
11. 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report.
Wu M; Zheng X; Wang X; Zhang G; Kuang J
BMC Med Genomics; 2020 Mar; 13(1):31. PubMed ID: 32126996
[TBL] [Abstract][Full Text] [Related]
12. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
Abu-Amero KK; Hellani AM; Salih MA; Seidahmed MZ; Elmalik TS; Zidan G; Bosley TM
BMC Med Genet; 2010 Sep; 11():135. PubMed ID: 20858261
[TBL] [Abstract][Full Text] [Related]
13. [Application of array-CGH and MLPA for detection of 4 cryptic unbalanced translocations].
Geng Q; Wu W; Luo F; Xu Z; Chen W; Li F; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):288-92. PubMed ID: 23744316
[TBL] [Abstract][Full Text] [Related]
14. Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion.
Roselló M; Monfort S; Orellana C; Ferrer-Bolufer I; Quiroga R; Oltra S; Martínez F
Cytogenet Genome Res; 2009; 125(2):103-8. PubMed ID: 19729912
[TBL] [Abstract][Full Text] [Related]
15. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
16. De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case report.
Al Dhaibani MA; Allingham-Hawkins D; El-Hattab AW
BMC Med Genet; 2017 Oct; 18(1):118. PubMed ID: 29061174
[TBL] [Abstract][Full Text] [Related]
17. Neurological expression of an inherited translocation of chromosomal 1 and 7.
AlMajhad NA; AlHashem AM; Bouhjar IA; Tabarki BM
Neurosciences (Riyadh); 2017 Jan; 22(1):62-64. PubMed ID: 28064333
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
19. A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesis.
Andrieux J; Cuvellier JC; Duban-Bedu B; Joriot-Chekaf S; Dieux-Coeslier A; Manouvrier-Hanu S; Delobel B; Vallee L
Eur J Med Genet; 2008; 51(1):87-91. PubMed ID: 18053786
[TBL] [Abstract][Full Text] [Related]
20. 1p36 deletion syndrome confirmed by fluorescence
Kang DS; Shin E; Yu J
Korean J Pediatr; 2016 Nov; 59(Suppl 1):S14-S18. PubMed ID: 28018437
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
