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Chondrodysplasia punctata and maternal systemic lupus erythematosus.

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

http://www.wikidata.org/entity/Q33681194

about

Chondrodysplasia punctata stemming from maternal lupus erythematosus.Maternal mixed connective tissue disease and offspring with chondrodysplasia punctata.Fetal chondrodysplasia punctata associated with maternal autoimmune diseases: a review.

P2860

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P2860

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

http://www.wikidata.org/entity/Q33681194

description

1998 nî lūn-bûn

@nan

1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@ast

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@en

type

label

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@ast

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@en

prefLabel

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@ast

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@en

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P1433

Journal of Medical Genetics

P1476

Chondrodysplasia punctata and maternal systemic lupus erythematosus.

@en

P2093

Toriello HV

http://www.w3.org/2001/XMLSchema#string

P2860

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders

A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

Maternal systemic lupus erythematosus and chondrodysplasia punctata in two sibs: phenocopy or coincidence?

Neonatal lupus syndrome: a case with chondrodysplasia punctata and other unusual manifestations.

Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders.

Punctate epiphyses: a radiological sign not a disease.

Prenatal exposure to phenytoin, facial development, and a possible role for vitamin K.

X-linked dominant ichthyosis with peroxisomal deficiency. An ultrastructural and ultracytochemical study of the Conradi-Hünermann syndrome and its murine homologue, the bare patches mouse.

P304

698-699

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scholarly article

P356

10.1136/JMG.35.8.698

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P407

P433

8

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35

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1998-08-01T00:00:00Z

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13566890

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9719384

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P932

1051403

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