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24. Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome. Conlin LK; Kaur M; Izumi K; Campbell L; Wilkens A; Clark D; Deardorff MA; Zackai EH; Pallister P; Hakonarson H; Spinner NB; Krantz ID Am J Med Genet A; 2012 Dec; 158A(12):3046-53. PubMed ID: 23169773 [TBL] [Abstract][Full Text] [Related]
25. Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype. Leube B; Majewski F; Gebauer J; Royer-Pokora B Am J Med Genet A; 2003 Dec; 123A(3):296-300. PubMed ID: 14608653 [TBL] [Abstract][Full Text] [Related]
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33. Unclassifiable pattern of hypopigmentation in a patient with mosaic partial 12p tetrasomy without Pallister-Killian syndrome. Alesi V; Dentici ML; Restaldi F; Orlando V; Liambo MT; Calacci C; Capolino R; Digilio MC; El Hachem M; Novelli A; Diociaiuti A; Dallapiccola B Am J Med Genet A; 2017 Jul; 173(7):1943-1946. PubMed ID: 28489314 [TBL] [Abstract][Full Text] [Related]
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