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Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome
Authors: Woods, C. G.; Stricker, S.; Seemann, P.; Stern, R.; Cox, J.; Sherridan, E.; Roberts, E.; Springell, K.; Scott, S.; Karbani, G.; Sharif, S. M.; Toomes, C.; Bond, J.; Kumar, D.; Al-Gazali, L.; Mundlos, Stefan
Date of Publication (YYYY-MM-DD): 2006-08
Title of Journal: American Journal of Human Genetics (Chicago, IL)
Volume: 79
Issue / Number: 2
Start Page: 402
End Page: 408
Document Type: Article
ID: 313095.0

Primary microcephaly: a centrosomal disease?
Authors: Cox, J.; Stern, R.; Springell, K.; Lindsay, S.; Scott, S.; Bond, Jacquelyn; Enard, Wolfgang; Woods, C. Geoffrey
Date of Publication (YYYY-MM-DD): 2005-09
Title of Journal: Journal of Medical Genetics
Volume: 42
Start Page: S34
End Page: S34
Document Type: Article
ID: 251524.0