[Spontaneous abortion of male fetuses with incontinentia pigmenti (apropos of a family)].
S. Odent(CIC Rennes), Anouk Borg, Asma Smahi(Délégation Paris 5), C Hors-Cayla, J Milon, M. C. Laurent, H Jouan, B. Le Marec(Hôpital Pontchaillou)
PubMed
January 1, 1997
Cited by 5
Related Papers
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
|Science|2007|1.1k
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
|Nature Genetics|2001|819
Mutation update for the <i>CSB</i> / <i>ERCC6</i> and <i>CSA</i> / <i>ERCC8</i> genes involved in Cockayne syndrome
|Human Mutation|2009|231
Perinatal‐lethal Gaucher disease
|American Journal of Medical Genetics Part A|2003|127
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
|Human Molecular Genetics|2013|112