147 related articles for article (PubMed ID: 32725750)
1. Speech and language development in children with 49,XXXXY syndrome.
Samango-Sprouse CA; Lasutschinkow PC; McLeod M; Porter GF; Powell S; St Laurent J; Sadeghin T; Gropman AL
Am J Med Genet A; 2021 Dec; 185(12):3567-3575. PubMed ID: 32725750
[TBL] [Abstract][Full Text] [Related]
2. 49,XXXXY syndrome: A study of neurological function in this uncommon X and Y chromosomal disorder.
Samango-Sprouse C; Lasutschinkow PC; Mitchell F; Porter GF; Hendrie P; Powell S; Sadeghin T; Gropman A
Am J Med Genet A; 2021 Dec; 185(12):3557-3566. PubMed ID: 32656941
[TBL] [Abstract][Full Text] [Related]
3. Neurocognitive development and capabilities in boys with 49,XXXXY syndrome.
Gropman AL; Porter GF; Lasutschinkow PC; Sadeghin T; Tipton ES; Powell S; Samango-Sprouse CA
Am J Med Genet A; 2021 Dec; 185(12):3541-3546. PubMed ID: 32662248
[TBL] [Abstract][Full Text] [Related]
4. Expanding the phenotypic profile of Kleefstra syndrome: A female with low-average intelligence and childhood apraxia of speech.
Samango-Sprouse C; Lawson P; Sprouse C; Stapleton E; Sadeghin T; Gropman A
Am J Med Genet A; 2016 May; 170A(5):1312-6. PubMed ID: 26833960
[TBL] [Abstract][Full Text] [Related]
5. DNA methylation and behavioral dysfunction in males with 47,XXY and 49,XXXXY: a pilot study.
Lee RS; Song SQ; Garrison-Desany HM; Carey JL; Lasutschinkow P; Zabel A; Bressler J; Gropman A; Samango-Sprouse C
Clin Epigenetics; 2021 Jul; 13(1):136. PubMed ID: 34210361
[TBL] [Abstract][Full Text] [Related]
6. Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.
Mei C; Fedorenko E; Amor DJ; Boys A; Hoeflin C; Carew P; Burgess T; Fisher SE; Morgan AT
Eur J Hum Genet; 2018 May; 26(5):676-686. PubMed ID: 29445122
[TBL] [Abstract][Full Text] [Related]
7. Prelinguistic communication development in children with childhood apraxia of speech: a retrospective analysis.
Highman C; Leitão S; Hennessey N; Piek J
Int J Speech Lang Pathol; 2012 Feb; 14(1):35-47. PubMed ID: 22257070
[TBL] [Abstract][Full Text] [Related]
8. Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY.
Visootsak J; Rosner B; Dykens E; Tartaglia N; Graham JM
Am J Med Genet A; 2007 Jun; 143A(11):1198-203. PubMed ID: 17497714
[TBL] [Abstract][Full Text] [Related]
9. Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia.
Morgan AT; Haaften LV; van Hulst K; Edley C; Mei C; Tan TY; Amor D; Fisher SE; Koolen DA
Eur J Hum Genet; 2018 Jan; 26(1):75-84. PubMed ID: 29225339
[TBL] [Abstract][Full Text] [Related]
10. The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.
Centanni TM; Sanmann JN; Green JR; Iuzzini-Seigel J; Bartlett C; Sanger WG; Hogan TP
Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):536-43. PubMed ID: 26097074
[TBL] [Abstract][Full Text] [Related]
11. [Gonosomal trisomy syndrome. Five case reports and review of literature].
Schwemmle C; Jungheim M; Ptok M
Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211
[TBL] [Abstract][Full Text] [Related]
12. Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX.
Samango-Sprouse C; Keen C; Mitchell F; Sadeghin T; Gropman A
Am J Med Genet A; 2015 Oct; 167A(10):2251-9. PubMed ID: 26086740
[TBL] [Abstract][Full Text] [Related]
13. Comorbidity and Severity in Childhood Apraxia of Speech: A Retrospective Chart Review.
Chenausky KV; Baas B; Stoeckel R; Brown T; Green JR; Runke C; Schimmenti L; Clark H
J Speech Lang Hear Res; 2023 Mar; 66(3):791-803. PubMed ID: 36795544
[TBL] [Abstract][Full Text] [Related]
14. CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases.
Morison LD; van Reyk O; Forbes E; Rouxel F; Faivre L; Bruinsma F; Vincent M; Jacquemont ML; Dykzeul NL; Geneviève D; Amor DJ; Morgan AT
Eur J Hum Genet; 2023 Jul; 31(7):793-804. PubMed ID: 36599938
[TBL] [Abstract][Full Text] [Related]
15. Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndrome.
Counts DR; Yu C; Lasutschinkow PC; Sadeghin T; Gropman A; Samango-Sprouse CA
Am J Med Genet A; 2021 Dec; 185(12):3547-3553. PubMed ID: 32618131
[TBL] [Abstract][Full Text] [Related]
16. Beyond 'speech delay': Expanding the phenotype of BRPF1-related disorder.
Morison LD; Van Reyk O; Baker E; Ruaud L; Couque N; Verloes A; Amor DJ; Morgan AT
Eur J Med Genet; 2024 Apr; 68():104923. PubMed ID: 38346666
[TBL] [Abstract][Full Text] [Related]
17. Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety-related symptoms and intact social awareness.
Lasutschinkow PC; Gropman AL; Porter GF; Sadeghin T; Samango-Sprouse CA
Am J Med Genet A; 2020 May; 182(5):974-986. PubMed ID: 32083381
[TBL] [Abstract][Full Text] [Related]
18. Early development in infants at risk of childhood apraxia of speech: a longitudinal investigation.
Highman C; Hennessey NW; Leitão S; Piek JP
Dev Neuropsychol; 2013; 38(3):197-210. PubMed ID: 23573797
[TBL] [Abstract][Full Text] [Related]
19. The behavioral profile of 49,XXXXY and the potential impact of testosterone replacement therapy.
Samango-Sprouse CA; Hamzik MP; Gropman E; Brooks MR; Powell S; Taylor AM; Sadeghin T; Gropman AL
Genet Med; 2023 Jul; 25(7):100847. PubMed ID: 37061875
[TBL] [Abstract][Full Text] [Related]
20. Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies.
Thompson T; Howell S; Davis S; Wilson R; Janusz J; Boada R; Pyle L; Tartaglia N
Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):414-427. PubMed ID: 32449585
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]