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Article

Sporadic neonatal Fanconi's anemia with VACTERL association.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Feb 2010

Kanemoto Nobuko, Fukushima Takashi, Imoto Natsuki, Koike Kazutoshi, Kanemoto Katsuyoshi, Matsuura Shinya

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Identifiers

PMID: 20158659
DOI: 10.1111/j.1442-200X.2009.02945.x

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Sporadic neonatal Fanconi's anemia with VACTERL association.PMID 20158659Read ↗

Possible form of Fanconi pancytopenia as a phenocopy of the VACTERL association.Semantic proximity Read ↗

Evidence for inheritance in patients with VACTERL associationSemantic proximity Read ↗

Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.Semantic proximity Read ↗

Phenotypic diversity of patients diagnosed with VACTERL association.Semantic proximity Read ↗

Clinical, cytogenetic, environmental and inheritance findings in Mexican neonates with VACTERL association.Semantic proximity Read ↗

Sporadic VACTERL association in a Japanese family with Sjögren-Larsson syndrome.Semantic proximity Read ↗

Novel FANCI mutations in Fanconi anemia with VACTERL association.Semantic proximity Read ↗

VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5.Semantic proximity Read ↗

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.Semantic proximity Read ↗

RAD51 -Related Fanconi Anemia: Expanding the Phenotypic Spectrum and Strong Association With VACTERL.Semantic proximity Read ↗

X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.Semantic proximity Read ↗

[VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?].Semantic proximity Read ↗

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