Chondrodysplasia punctata and maternal systemic lupus erythematosus.

Author:

Toriello H V

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Neonatal lupus syndrome: a and other unusual mcaansiefewstiatthiocnhso.nd7roMdeydsplGaensiieat punctata 1998; 35: 695-7. 7-dehydrocholesterol metabolism. In yet other conditions in which CP can occur (for example, trisomies 18 and 21, fetal alcohol or;Austin-Ward, E.; Castillo, S.; Cuchacovich, M.

2. Brachytelephalangic chondrodysplasia punctata in an extremely premature infant;Mansour, S.; Liberman, D.; Young, I.;Am Med Genet,1994

3. Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders;Wulfsberg, E.A.; Curtis, J.; Jayne, C.H.;Am Med Genet,1992

4. Punctate epiphyses: a radiologic sign not a disease;Poznanski, A.K.;Pediatr Radiol,1994

5. deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism;Menger, H.; Lin, A.E.; Toriello, H.V.;Am J7Med Genet,1997

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