✦ LIBER ✦

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

✍ Scribed by Dr Stephen G. Ryan; Max Wiznitzer; Charlotte Hollman; M. Cristina Torres; Maria Szekeresova; Sandra Schneider

Publisher: John Wiley and Sons
Year: 1991
Tongue: English
Weight: 479 KB
Volume: 29
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.410290504

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Familial exudative vitreoretinopathy: Fu

Familial exudative vitreoretinopathy: Further evidence for genetic heterogeneity

✍ Shastry, Barkur S.; Trese, Michael T. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 176 KB 👁 1 views

Evidence for genetic heterogeneity in fa

Evidence for genetic heterogeneity in familial isolated patella aplasia-hypoplasia

✍ Bongers, Ernie M.H.F. ;van Bokhoven, Hans ;Knoers, Nine V.A.M. ;Hamel, Ben C.J. 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 76 KB

Association between tumor necrosis facto

Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: Evidence for genetic heterogeneity

✍ Philippe Dieudé; Elisabeth Petit; Séverine Cailleau-Moindrault; José Osorio; Cél 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 71 KB 👁 2 views

De novo CIAS1 mutations, cytokine activa

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases

✍ Ivona Aksentijevich; Miroslawa Nowak; Mustapha Mallah; Jae Jin Chae; Wendy T. Wa 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 350 KB 👁 2 views