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Items: 2

1.

Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.

Slavotinek A, Lee SS, Davis R, Shrit A, Leppig KA, Rhim J, Jasnosz K, Albertson D, Pinkel D.

J Med Genet. 2005 Sep;42(9):730-6.

2.

Myeloperoxidase deficiency and severe sepsis.

Grossl NA, Candel AG, Shrit A, Schumacher HR.

South Med J. 1993 Jul;86(7):832-6.

PMID:
8391723

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