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.
29. 47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome. Fryns JP, Kleczkowska A, Van den Berghe H. Ann Genet; 1986; 29(2):112-3. PubMed ID: 3490205 [Abstract] [Full Text] [Related]
38. Simpson-Golabi-Behmel syndrome: a prenatal diagnosis in a foetus with GPC3 and GPC4 gene microduplications. Mujezinović F, Krgović D, Blatnik A, Zagradišnik B, Vipotnik TV, Golec T, Tul N, Vokač NK. Clin Genet; 2016 Jul; 90(1):99-101. PubMed ID: 26847959 [No Abstract] [Full Text] [Related]