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Cited by
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This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Slavotinek, A Gaunt, L and Donnai, D 1997. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.. Journal of Medical Genetics, Vol. 34, Issue. 10, p. 819.
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Benzacken, Brigitte Monier-Gavelle, Fr�d�rique Pierre Siffroi, Jean Agbo, Placide Chalvon, Arnaud and Philippe Wolf, Jean 2001. Acrocentric chromosome polymorphisms: beware of cryptic translocations. Prenatal Diagnosis, Vol. 21, Issue. 2, p. 96.
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Witkowski, Regine Prokop, Otto Ullrich, Eva and Thiel, Gundula 2003. Lexikon der Syndrome und Fehlbildungen. p. 31.
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Roberts, Amy E. Cox, Gerald F. Kimonis, Virginia Lamb, Allen and Irons, Mira 2004. Clinical presentation of 13 patients with subtelomeric rearrangements and a review of the literature. American Journal of Medical Genetics Part A, Vol. 128A, Issue. 4, p. 352.
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Lebiedzińska, Aneta 2008. Poradnictwo genetyczne w zespole Beckwitha-Wiedemanna. Część I. Diagnoza fenotypowa i genetyczna. Pediatria Polska, Vol. 83, Issue. 5, p. 529.
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Lekszas, Caroline Nanda, Indrajit Vona, Barbara Böck, Julia Ashrafzadeh, Farah Donyadideh, Nahid Ebrahimzadeh, Farnoosh Ahangari, Najmeh Maroofian, Reza Karimiani, Ehsan Ghayoor and Haaf, Thomas 2019. Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report. BMC Medical Genomics, Vol. 12, Issue. 1,
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A New Case of Beckwith-Wiedemann Syndrome with an 11p15 Duplication of Paternal Origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]
  • Volume 45, Issue 1-2
  • M. Krajewska-Walasek (a1), A. Gutkowska (a1), M. Mospinek-Krasnopolska (a1) and K. Chrzanowska (a1)
  • DOI: https://doi.org/10.1017/S0001566000001392
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A New Case of Beckwith-Wiedemann Syndrome with an 11p15 Duplication of Paternal Origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]
  • Volume 45, Issue 1-2
  • M. Krajewska-Walasek (a1), A. Gutkowska (a1), M. Mospinek-Krasnopolska (a1) and K. Chrzanowska (a1)
  • DOI: https://doi.org/10.1017/S0001566000001392
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A New Case of Beckwith-Wiedemann Syndrome with an 11p15 Duplication of Paternal Origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]
  • Volume 45, Issue 1-2
  • M. Krajewska-Walasek (a1), A. Gutkowska (a1), M. Mospinek-Krasnopolska (a1) and K. Chrzanowska (a1)
  • DOI: https://doi.org/10.1017/S0001566000001392
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