153 related articles for article (PubMed ID: 26893599)
1. Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.
Seo GH; Kim JH; Cho JH; Kim GH; Seo EJ; Lee BH; Choi JH; Yoo HW
Korean J Pediatr; 2016 Jan; 59(1):16-23. PubMed ID: 26893599
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
[TBL] [Abstract][Full Text] [Related]
4. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
5. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
6. Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations.
Chaudhry C; Kumari D; Panigrahi I; Kaur P
J Pediatr Genet; 2023 Dec; 12(4):342-347. PubMed ID: 38162157
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
Hussen DF; Kamel AK; Mekkawy MK; Ashaat EA; El Ruby MO
Mol Syndromol; 2020 Dec; 11(5-6):284-295. PubMed ID: 33510599
[TBL] [Abstract][Full Text] [Related]
8. Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental Delay.
Srivastava P; Kaur P; Daniel R; Chaudhry C; Kaur A; Seth S; Kumari D; Kaur A; Panigrahi I
J Pediatr Genet; 2024 Jun; 13(2):81-89. PubMed ID: 38721576
[TBL] [Abstract][Full Text] [Related]
9. Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review.
Greco M; Ferrara P; Farello G; Striano P; Verrotti A
Epilepsy Res; 2018 Jan; 139():92-101. PubMed ID: 29212048
[TBL] [Abstract][Full Text] [Related]
10. Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S; Beneteau C; Redon S; Dupont C; Missirian C; Jaeger P; Herve B; Jacquin C; Douet-Guilbert N; Till M; Tabet AC; Moradkhani K; Malan V; Doco-Fenzy M; Vialard F
Prenat Diagn; 2019 Sep; 39(10):871-882. PubMed ID: 31172545
[TBL] [Abstract][Full Text] [Related]
11. Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
Yokoyama E; Villarroel CE; Diaz S; Del Castillo V; Pérez-Vera P; Salas C; Gómez S; Barreda R; Molina B; Frias S
Mol Cytogenet; 2020; 13():42. PubMed ID: 32939224
[TBL] [Abstract][Full Text] [Related]
12. Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment-A Case Report.
Briegel W
Int J Environ Res Public Health; 2021 Nov; 18(22):. PubMed ID: 34831818
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology].
Laczmańska I; Jakubiak A; Slęzak R; Pesz K; Stembalska A; Laczmański L; Sąsiadek MM; Smigiel R
Med Wieku Rozwoj; 2011; 15(2):132-9. PubMed ID: 22002044
[TBL] [Abstract][Full Text] [Related]
15. Monosomy 1p36.
Slavotinek A; Shaffer LG; Shapira SK
J Med Genet; 1999 Sep; 36(9):657-63. PubMed ID: 10507720
[TBL] [Abstract][Full Text] [Related]
16. 576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.
Zhu X; Zhang Y; Wang J; Yang JF; Yang YF; Tan ZP
Gene; 2013 Oct; 528(2):352-5. PubMed ID: 23892090
[TBL] [Abstract][Full Text] [Related]
17. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.
Isidor B; Le Cunff M; Boceno M; Boisseau P; Thomas C; Rival JM; David A; Le Caignec C
Eur J Med Genet; 2008; 51(6):679-84. PubMed ID: 18672103
[TBL] [Abstract][Full Text] [Related]
18. A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation.
Dincsoy Bir F; Silan F; Velickovic J; Berkay Akcan M; Ozdemir O
Mol Syndromol; 2022 May; 13(3):254-260. PubMed ID: 35707596
[TBL] [Abstract][Full Text] [Related]
19. Clinical and neuroradiological features of the 9p deletion syndrome.
Spazzapan P; Arnaud E; Baujat G; Nizon M; Malan V; Brunelle F; Di Rocco F
Childs Nerv Syst; 2016 Feb; 32(2):327-35. PubMed ID: 26597681
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]