130 related articles for article (PubMed ID: 38831650)
1. Special clinical entity with 15q26 deletion: a novel case report.
Panteleev D; Sadova A; Pavlova G
J Genet; 2024; 103():. PubMed ID: 38831650
[TBL] [Abstract][Full Text] [Related]
2. Extraction of genomic DNA for sequencing from snail
Liu WL; Li F; Liu L; Ai R
J Genet; 2024; 103():. PubMed ID: 38831651
[TBL] [Abstract][Full Text] [Related]
3. 15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.
Benbouchta Y; De Leeuw N; Amasdl S; Sbiti A; Smeets D; Sadki K; Sefiani A
Ital J Pediatr; 2021 Sep; 47(1):188. PubMed ID: 34530895
[TBL] [Abstract][Full Text] [Related]
4. De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes.
Tönnies H; Schulze I; Hennies H; Neumann LM; Keitzer R; Neitzel H
J Med Genet; 2001 Sep; 38(9):617-21. PubMed ID: 11565548
[No Abstract] [Full Text] [Related]
5. Identification of Immediate Early Genes in the Nervous System of Snail
Xu C; Li Q; Efimova O; Jiang X; Petrova M; K Vinarskaya A; Kolosov P; Aseyev N; Koshkareva K; Ierusalimsky VN; Balaban PM; Khaitovich P
eNeuro; 2019; 6(3):. PubMed ID: 31053606
[TBL] [Abstract][Full Text] [Related]
6. Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case.
Veredice C; Bianco F; Contaldo I; Orteschi D; Stefanini MC; Battaglia D; Lettori D; Guzzetta F; Zollino M
Epilepsia; 2009 Jul; 50(7):1810-5. PubMed ID: 19486360
[TBL] [Abstract][Full Text] [Related]
7. Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance.
O'Riordan AM; McGrath N; Sharif F; Murphy NP; Franklin O; Lynch SA; O'Grady MJ
Eur J Pediatr; 2017 Jan; 176(1):137-142. PubMed ID: 27826649
[TBL] [Abstract][Full Text] [Related]
8. Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.
Szabó A; Czakó M; Hadzsiev K; Duga B; Bánfai Z; Komlósi K; Melegh B
Am J Med Genet A; 2018 Feb; 176(2):443-449. PubMed ID: 29226546
[TBL] [Abstract][Full Text] [Related]
9. Kidney abnormalities in persons with monosomy 15q26.
Lurie IW
Am J Med Genet A; 2008 Jul; 146A(13):1761-4. PubMed ID: 18512227
[No Abstract] [Full Text] [Related]
10. Terminal deletion of chromosome 15q26.1: case report and brief literature review.
Bhakta KY; Marlin SJ; Shen JJ; Fernandes CJ
J Perinatol; 2005 Jun; 25(6):429-32. PubMed ID: 15843813
[TBL] [Abstract][Full Text] [Related]
11. Microdeletion of chromosome 15q26.1 in a child with intractable generalized epilepsy.
Dhamija R; Breningstall G; Wong-Kisiel L; Dolan M; Hirsch B; Wirrell E
Pediatr Neurol; 2011 Jul; 45(1):60-2. PubMed ID: 21723464
[TBL] [Abstract][Full Text] [Related]
12. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
Pujana MA; Nadal M; Gratacòs M; Peral B; Csiszar K; González-Sarmiento R; Sumoy L; Estivill X
Genome Res; 2001 Jan; 11(1):98-111. PubMed ID: 11156619
[TBL] [Abstract][Full Text] [Related]
13. Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qter.
Poot M; Eleveld MJ; van 't Slot R; van Genderen MM; Verrijn Stuart AA; Hochstenbach R; Beemer FA
Eur J Med Genet; 2007; 50(6):432-40. PubMed ID: 17931990
[TBL] [Abstract][Full Text] [Related]
14. Phenoloxidase is involved in the immune reaction of Helix lucorum to parasitic infestation by dicrocoeliid trematode.
Unlu AH; Ekici A
Ann Agric Environ Med; 2021 Sep; 28(3):426-429. PubMed ID: 34558265
[TBL] [Abstract][Full Text] [Related]
15. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.
Slavotinek AM; Moshrefi A; Davis R; Leeth E; Schaeffer GB; Burchard GE; Shaw GM; James B; Ptacek L; Pennacchio LA
Eur J Hum Genet; 2006 Sep; 14(9):999-1008. PubMed ID: 16736036
[TBL] [Abstract][Full Text] [Related]
16. Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature.
Klaassens M; Galjaard RJ; Scott DA; Brüggenwirth HT; van Opstal D; Fox MV; Higgins RR; Cohen-Overbeek TE; Schoonderwaldt EM; Lee B; Tibboel D; de Klein A
Am J Med Genet A; 2007 Sep; 143A(18):2204-12. PubMed ID: 17702015
[TBL] [Abstract][Full Text] [Related]
17. Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings.
Dello Russo P; Demori E; Sechi A; Passon N; Romagno D; Gnan C; Zoratti R; Damante G
Cytogenet Genome Res; 2016; 148(1):14-8. PubMed ID: 27160288
[TBL] [Abstract][Full Text] [Related]
18. Characterisation of neurofilament protein NF70 mRNA from the gastropod Helix aspersa reveals that neuronal and non-neuronal intermediate filament proteins of cerebral ganglia arise from separate lamin-related genes.
Adjaye J; Plessmann U; Weber K; Dodemont H
J Cell Sci; 1995 Nov; 108 ( Pt 11)():3581-90. PubMed ID: 8586669
[TBL] [Abstract][Full Text] [Related]
19. [Chromosome aberration in a full-term neonate with low birth weight using microarray comparative genomic hybridization].
Sun S; Luo F; He J; Chen W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):550-4. PubMed ID: 18841570
[TBL] [Abstract][Full Text] [Related]
20. Recurrent enlarged nuchal translucency: first trimester presentation of a familial 15q26→qter deletion.
Reiss R; Ahern D; Sandstrom M; Wilkins-Haug L
Am J Med Genet A; 2015 Mar; 167A(3):612-6. PubMed ID: 25691414
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]