An Infrequent Double Mutation in the MEN1 Gene

G. Pérez de Nanclares,; L. Castano,; J.R. Bilbao,; S. Gaztambide,

doi:10.1515/IJDHD.2001.2.4.241

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An Infrequent Double Mutation in the MEN1 Gene

G. Pérez de Nanclares, , L. Castano, , J.R. Bilbao, and S. Gaztambide,

Published/Copyright: October 1, 2001

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From the journal International Journal on Disability and Human Development Volume 2 Issue 4

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Harvard
Chicago
Vancouver

de Nanclares,, G. Pérez, Castano,, L., Bilbao,, J.R. and Gaztambide,, S.. "An Infrequent Double Mutation in the MEN1 Gene" International Journal on Disability and Human Development, vol. 2, no. 4, pp. 241-246. https://doi.org/10.1515/IJDHD.2001.2.4.241

de Nanclares,, G., Castano,, L., Bilbao,, J. & Gaztambide,, S. (). An Infrequent Double Mutation in the MEN1 Gene. International Journal on Disability and Human Development, 2(4), 241-246. https://doi.org/10.1515/IJDHD.2001.2.4.241

de Nanclares,, G., Castano,, L., Bilbao,, J. and Gaztambide,, S. () An Infrequent Double Mutation in the MEN1 Gene. International Journal on Disability and Human Development, Vol. 2 (Issue 4), pp. 241-246. https://doi.org/10.1515/IJDHD.2001.2.4.241

de Nanclares,, G. Pérez, Castano,, L., Bilbao,, J.R. and Gaztambide,, S.. "An Infrequent Double Mutation in the MEN1 Gene" International Journal on Disability and Human Development 2, no. 4 (): 241-246. https://doi.org/10.1515/IJDHD.2001.2.4.241

de Nanclares, G, Castano, L, Bilbao, J, Gaztambide, S. An Infrequent Double Mutation in the MEN1 Gene. International Journal on Disability and Human Development. ;2(4): 241-246. https://doi.org/10.1515/IJDHD.2001.2.4.241

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Published Online: 2001-10

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Letter from the Editors
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Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
Adrenal Mass in Carney Triad
An Infrequent Double Mutation in the MEN1 Gene
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https://doi.org/10.1515/IJDHD.2001.2.4.241

Articles in the same Issue

CONTENTS
Letter from the Editors
Molecular Genetics of Thyroid Disorders in the Neonate: A Review
Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
Adrenal Mass in Carney Triad
An Infrequent Double Mutation in the MEN1 Gene
X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation
BOOK REVIEWS. CALENDAR. INDEX