Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
about
Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case reportInfantile Systemic Hyalinosis: Report of 17-year ExperienceInfantile systemic hyalinosis: a case report with a novel mutationHyaline Fibromatosis Syndrome: A Rare Inherited DisorderInfantile systemic hyalinosis: Report of two severe cases from Saudi Arabia and review of the literature.Identical Twins with Infantile Systemic Hyalinosis: Case study and review of literature.Infantile systemic hyalinosis in identical twins.
P2860
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P2860
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
description
2005 nî lūn-bûn
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name
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
@en
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
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type
label
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
@en
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
@nl
prefLabel
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
@en
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
@nl
P2093
P1476
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.
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P2093
P304
P577
2005-09-01T00:00:00Z