42 related articles for article (PubMed ID: 25661042)
1. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder.
Meza-Espinoza JP; Contreras-Gutiérrez JA; Arámbula-Meraz E; González-García JR; Domínguez-Quezada MG; García-Magallanes N; Madueña-Molina J; Benítez-Pascual J; Partida-Pérez M; Picos-Cárdenas VJ
Mol Cytogenet; 2021 Sep; 14(1):43. PubMed ID: 34481514
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of Autism Spectrum Disorders in Guanajuato, Mexico: The Leon survey.
Fombonne E; Marcin C; Manero AC; Bruno R; Diaz C; Villalobos M; Ramsay K; Nealy B
J Autism Dev Disord; 2016 May; 46(5):1669-85. PubMed ID: 26797939
[TBL] [Abstract][Full Text] [Related]
3. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Costain G; Walker S; Argiropoulos B; Baribeau DA; Bassett AS; Boot E; Devriendt K; Kellam B; Marshall CR; Prasad A; Serrano MA; Stavropoulos DJ; Twede H; Vermeesch JR; Vorstman JAS; Scherer SW
J Neurodev Disord; 2019 Feb; 11(1):3. PubMed ID: 30732576
[TBL] [Abstract][Full Text] [Related]
4. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
[TBL] [Abstract][Full Text] [Related]
5. Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2).
Lalani SR; Sahoo T; Sanders ME; Peters SU; Bejjani BA
BMC Med Genet; 2006 Feb; 7():8. PubMed ID: 16472378
[TBL] [Abstract][Full Text] [Related]
6. Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion.
Papadopoulou E; Sismani C; Christodoulou C; Ioannides M; Kalmanti M; Patsalis P
Am J Med Genet A; 2010 Jun; 152A(6):1515-22. PubMed ID: 20503328
[TBL] [Abstract][Full Text] [Related]
7. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
[TBL] [Abstract][Full Text] [Related]
8. Clinical and molecular characterization of a patient with 15q21.2q22.2 deletion syndrome.
Velázquez-Wong AC; Ruiz Esparza-Garrido R; Velázquez-Flores MÁ; Huicochea-Montiel JC; Cárdenas-Conejo A; Miguez-Muñoz CP; Araujo-Solís MA; Salamanca-Gómez F; Arenas-Aranda DJ
Cytogenet Genome Res; 2014; 144(3):183-9. PubMed ID: 25661042
[TBL] [Abstract][Full Text] [Related]
9. An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature.
L Ng IS; Chin WH; P Lim EC; Tan EC
Twin Res Hum Genet; 2011 Aug; 14(4):333-9. PubMed ID: 21787116
[TBL] [Abstract][Full Text] [Related]
10. Deletion 2p15-16.1 syndrome: case report and review.
Prontera P; Bernardini L; Stangoni G; Capalbo A; Rogaia D; Romani R; Ardisia C; Dallapiccola B; Donti E
Am J Med Genet A; 2011 Oct; 155A(10):2473-8. PubMed ID: 21910216
[TBL] [Abstract][Full Text] [Related]
11. Deletion 21pterq22.11: Report of a Patient with Dysmorphic Features, Hypertonia, and Café-au-Lait Macules and Review of the Literature.
Malinverni ACM; Yamashiro Coelho ÉM; Chen K; Colovati ME; Soares Pinho Cernach MC; Bragagnolo S; Melaragno MI
Cytogenet Genome Res; 2017; 153(2):81-85. PubMed ID: 29258104
[TBL] [Abstract][Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No 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]