Apparent cyclophosphamide (cytoxan) embryopathy: a distinct phenotype?

Enns, G M; Roeder, E; Chan, R T; Ali-Khan Catts, Z; Cox, V A; Golabi, M

Enns, G M; Roeder, E; Chan, R T; Ali-Khan Catts, Z; Cox, V A; Golabi, M.

Affiliation

Enns GM; Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, California.

Am J Med Genet ; 86(3): 237-41, 1999 Sep 17.

Article in En | MEDLINE | ID: mdl-10482872

Subject(s)

Abnormalities, Multiple/chemically induced; Cyclophosphamide/adverse effects; Abnormalities, Multiple/pathology; Adult; Animals; Blepharophimosis/chemically induced; Craniosynostoses/chemically induced; Developmental Disabilities/chemically induced; Ear, External/abnormalities; Female; Growth Disorders/chemically induced; Humans; Infant, Newborn; Limb Deformities, Congenital/chemically induced; Lupus Erythematosus, Systemic/complications; Lupus Erythematosus, Systemic/drug therapy; Maternal-Fetal Exchange; Phenotype; Pregnancy; Pregnancy Complications/drug therapy; Teratogens/toxicity

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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Cyclophosphamide Type of study: Risk_factors_studies Limits: Adult / Animals / Female / Humans / Newborn / Pregnancy Language: En Journal: Am J Med Genet Year: 1999 Document type: Article

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