These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
136 related articles for article (PubMed ID: 25624931)
1. Baraitser and Winter syndrome with growth hormone deficiency. Chentli F; Zellagui H J Pediatr Neurosci; 2014; 9(3):257-9. PubMed ID: 25624931 [TBL] [Abstract][Full Text] [Related]
2. New ocular finding in Baraitser-Winter syndrome (BWS). Rall N; Leon A; Gomez R; Daroca J; Lacassie Y Eur J Med Genet; 2018 Jan; 61(1):21-23. PubMed ID: 29024830 [TBL] [Abstract][Full Text] [Related]
3. The First Korean Case of Baraitser-Winter Cerebro-Fronto-Facial Syndrome with a Novel Mutation in Choi GJ; Kim MS; Park H; Kim JY; Choi JM; Lee SM; Jang JH; Cho SY; Jin DK Ann Clin Lab Sci; 2020 Nov; 50(6):818-824. PubMed ID: 33334799 [TBL] [Abstract][Full Text] [Related]
11. Cerebro-fronto-facial syndrome type 3 with polymicrogyria: a clinical presentation of Baraitser-Winter syndrome. Eker HK; Derinkuyu BE; Ünal S; Masliah-Planchon J; Drunat S; Verloes A Eur J Med Genet; 2014 Jan; 57(1):32-6. PubMed ID: 24211661 [TBL] [Abstract][Full Text] [Related]
12. The phenotypic spectrum of baraitser-winter syndrome: a new case and review of literature. Ganesh A; Al-Kindi A; Jain R; Raeburn S J AAPOS; 2005 Dec; 9(6):604-6. PubMed ID: 16414535 [TBL] [Abstract][Full Text] [Related]
13. Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome. Cianci P; Fazio G; Casagranda S; Spinelli M; Rizzari C; Cazzaniga G; Selicorni A Am J Med Genet A; 2017 Feb; 173(2):546-549. PubMed ID: 27868373 [TBL] [Abstract][Full Text] [Related]
14. Iris coloboma, ptosis, hypertelorism, and mental retardation: Baraitser-Winter syndrome or Noonan syndrome? Verloes A J Med Genet; 1993 May; 30(5):425-6. PubMed ID: 8320709 [TBL] [Abstract][Full Text] [Related]
15. Identification of a Nie K; Huang J; Liu L; Lv H; Chen D; Fan W Front Genet; 2022; 13():828120. PubMed ID: 35401677 [TBL] [Abstract][Full Text] [Related]
16. De Novo Dawidziuk M; Kutkowska-Kazmierczak A; Bukowska-Olech E; Jurek M; Kalka E; Guilbride DL; Furmanek MI; Bekiesinska-Figatowska M; Bal J; Gawlinski P Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35054877 [TBL] [Abstract][Full Text] [Related]
17. Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations. Di Donato N; Rump A; Koenig R; Der Kaloustian VM; Halal F; Sonntag K; Krause C; Hackmann K; Hahn G; Schrock E; Verloes A Eur J Hum Genet; 2014 Feb; 22(2):179-83. PubMed ID: 23756437 [TBL] [Abstract][Full Text] [Related]
18. Previously undescribed phenotypic findings and novel ACTG1 gene pathogenic variants in Baraitser-Winter cerebrofrontofacial syndrome. Chacon-Camacho OF; Barragán-Arévalo T; Villarroel CE; Almanza-Monterrubio M; Zenteno JC Eur J Med Genet; 2020 May; 63(5):103877. PubMed ID: 32028042 [TBL] [Abstract][Full Text] [Related]