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Refinado por: Base de dados/Biblioteca: AUC Wiley Frozen Package in 2012 remover assunto: Life Sciences & Biomedicine remover Female remover Clinical Genetics remover
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Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
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Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?

Fujita, A. ; Waga, C. ; Hachiya, Y. ; Kurihara, E. ; Kumada, S. ; Takeshita, E. ; Nakagawa, E. ; Inoue, K. ; Miyatake, S. ; Tsurusaki, Y. ; Nakashima, M. ; Saitsu, H. ; Goto, Y.-i. ; Miyake, N. ; Matsumoto, N.

Clinical genetics, 2016-09, Vol.90 (3), p.276-281 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2
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Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2

Pyatt, RE ; Nakagawa, H ; Hampel, H ; Sedra, M ; Fuchik, MB ; Comeras, I ; De La Chapelle, A ; Prior, TW

Clinical genetics, 2003-03, Vol.63 (3), p.215-218 [Periódico revisado por pares]

Oxford, UK: Munksgaard International Publishers

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