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Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene.
J Pediatr. 1996 Jul;129(1):56-62. doi: 10.1016/s0022-3476(96)70190-7.
J Pediatr. 1996.
PMID: 8757563
Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.
Barrat FJ, Auloge L, Pastural E, Lagelouse RD, Vilmer E, Cant AJ, Weissenbach J, Le Paslier D, Fischer A, de Saint Basile G.
Barrat FJ, et al. Among authors: lagelouse rd.
Am J Hum Genet. 1996 Sep;59(3):625-32.
Am J Hum Genet. 1996.
PMID: 8751864
Free PMC article.
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