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Article

Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency.

Clinical dysmorphology - 1 Apr 2010

Alessandri Jean-Luc Dominique, Ramful Duksha, Cuillier Fabrice

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Identifiers

PMID: 20177377
DOI: 10.1097/MCD.0b013e328335c14a

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Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency.PMID 20177377Read ↗

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Brachytelephalangic chondrodysplasia punctata with distinctive phenotype and normal karyotype.Semantic proximity Read ↗

Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature.Semantic proximity Read ↗

Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata.Semantic proximity Read ↗

Binder phenotype: associated findings and etiologic mechanisms.Semantic proximity Read ↗

Prenatal diagnosis of cervical spinal cord compression in chondrodysplasia punctata brachytelephalangic type: A case report and literature review.Semantic proximity Read ↗

A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies.Semantic proximity Read ↗

Fetal Chondrodysplasia Punctata: A Clinical Study of Five CasesSemantic proximity Read ↗

Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: case report and review.Semantic proximity Read ↗

Brachytelephalangic chondrodysplasia punctata: a case series to further delineate the phenotype.Semantic proximity Read ↗

Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)Semantic proximity Read ↗

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