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Fryns Syndrome

Dec. 25, 2024

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Fryns syndrome: MedlinePlus Genetics
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Fryns syndrome: a case associated with kryotype XO | Annals of Saudi Medicine
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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the …
Fryns Syndrome: A Lethal Birth Defect with Variable Phenotypic Expressions in Sibli…
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Fryns Syndrome: Neurologic Findings in a Survivor | Semantic Scholar
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Recessive loss of function PIGN alleles, including an intragenic deletion with foun…
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