81 related articles for article (PubMed ID: 38572385)
1. Noonan syndrome on the African Continent.
Tekendo-Ngongang C; Kruszka P
Birth Defects Res; 2020 Jun; 112(10):718-724. PubMed ID: 32558383
[TBL] [Abstract][Full Text] [Related]
2. Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome.
Shoji Y; Hata A; Maeyama T; Wada T; Hasegawa Y; Nishi E; Ida S; Etani Y; Niihori T; Aoki Y; Okamoto N; Kawai M
Clin Pediatr Endocrinol; 2024; 33(2):50-58. PubMed ID: 38572385
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome patients with RIT1 mutations.
Yaoita M; Niihori T; Mizuno S; Okamoto N; Hayashi S; Watanabe A; Yokozawa M; Suzumura H; Nakahara A; Nakano Y; Hokosaki T; Ohmori A; Sawada H; Migita O; Mima A; Lapunzina P; Santos-Simarro F; García-Miñaúr S; Ogata T; Kawame H; Kurosawa K; Ohashi H; Inoue S; Matsubara Y; Kure S; Aoki Y
Hum Genet; 2016 Feb; 135(2):209-22. PubMed ID: 26714497
[TBL] [Abstract][Full Text] [Related]
4. Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.
Athota JP; Bhat M; Nampoothiri S; Gowrishankar K; Narayanachar SG; Puttamallesh V; Farooque MO; Shetty S
BMC Med Genet; 2020 Mar; 21(1):50. PubMed ID: 32164556
[TBL] [Abstract][Full Text] [Related]
5. The molecular genetics of RASopathies: An update on novel disease genes and new disorders.
Tartaglia M; Aoki Y; Gelb BD
Am J Med Genet C Semin Med Genet; 2022 Dec; 190(4):425-439. PubMed ID: 36394128
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.
Papadopoulos G; Papadopoulou A; Kosma K; Papadimitriou A; Papaevangelou V; Kanaka-Gantenbein C; Bountouvi E; Kitsiou-Tzeli S
Eur J Pediatr; 2022 Oct; 181(10):3691-3700. PubMed ID: 35904599
[TBL] [Abstract][Full Text] [Related]
7. Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1.
Uludağ Alkaya D; Lissewski C; Yeşil G; Zenker M; Tüysüz B
Am J Med Genet A; 2021 Dec; 185(12):3623-3633. PubMed ID: 34184824
[TBL] [Abstract][Full Text] [Related]
8. Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil.
Bertola DR; Castro MAA; Yamamoto GL; Honjo RS; Ceroni JR; Buscarilli MM; Freitas AB; Malaquias AC; Pereira AC; Jorge AAL; Passos-Bueno MR; Kim CA
Am J Med Genet C Semin Med Genet; 2020 Dec; 184(4):896-911. PubMed ID: 33128510
[TBL] [Abstract][Full Text] [Related]
9. Young children with Noonan syndrome: evaluation of feeding problems.
Draaisma JMT; Drossaers J; van den Engel-Hoek L; Leenders E; Geelen J
Eur J Pediatr; 2020 Nov; 179(11):1683-1688. PubMed ID: 32394265
[TBL] [Abstract][Full Text] [Related]
10. Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.
Shoji Y; Ida S; Niihori T; Aoki Y; Okamoto N; Etani Y; Kawai M
Endocr J; 2019 Nov; 66(11):983-994. PubMed ID: 31292302
[TBL] [Abstract][Full Text] [Related]
11. Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients.
Li X; Yao R; Tan X; Li N; Ding Y; Li J; Chang G; Chen Y; Ma L; Wang J; Fu L; Wang X
Clin Genet; 2019 Oct; 96(4):290-299. PubMed ID: 31219622
[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]
