Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene

M.P. Wajnrajch,; J.M. Gertner,; P.E. Mullis,; J. Deladoey,; J.D. Cogan,; S. Lekhakula,; S. Kim,; P.S. Dannies,; P. Saenger,; T. Moshang,; J.A. Phillips III,; R.L. Leibel,

doi:10.1515/IJDHD.2000.1.3.125

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Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene

M.P. Wajnrajch, , J.M. Gertner, , P.E. Mullis, , J. Deladoey, , J.D. Cogan, , S. Lekhakula, , S. Kim, , P.S. Dannies, , P. Saenger, , T. Moshang, , J.A. Phillips III, und R.L. Leibel,

Veröffentlicht/Copyright: 1. Juli 2000

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Aus der Zeitschrift International Journal on Disability and Human Development Band 1 Heft 3

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Wajnrajch,, M.P., Gertner,, J.M., Mullis,, P.E., Deladoey,, J., Cogan,, J.D., Lekhakula,, S., Kim,, S., Dannies,, P.S., Saenger,, P., Moshang,, T., Phillips III,, J.A. and Leibel,, R.L.. "Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene" International Journal on Disability and Human Development, vol. 1, no. 3, pp. 125-136. https://doi.org/10.1515/IJDHD.2000.1.3.125

Wajnrajch,, M., Gertner,, J., Mullis,, P., Deladoey,, J., Cogan,, J., Lekhakula,, S., Kim,, S., Dannies,, P., Saenger,, P., Moshang,, T., Phillips III,, J. & Leibel,, R. (). Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene. International Journal on Disability and Human Development, 1(3), 125-136. https://doi.org/10.1515/IJDHD.2000.1.3.125

Wajnrajch,, M., Gertner,, J., Mullis,, P., Deladoey,, J., Cogan,, J., Lekhakula,, S., Kim,, S., Dannies,, P., Saenger,, P., Moshang,, T., Phillips III,, J. and Leibel,, R. () Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene. International Journal on Disability and Human Development, Vol. 1 (Issue 3), pp. 125-136. https://doi.org/10.1515/IJDHD.2000.1.3.125

Wajnrajch,, M.P., Gertner,, J.M., Mullis,, P.E., Deladoey,, J., Cogan,, J.D., Lekhakula,, S., Kim,, S., Dannies,, P.S., Saenger,, P., Moshang,, T., Phillips III,, J.A. and Leibel,, R.L.. "Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene" International Journal on Disability and Human Development 1, no. 3 (): 125-136. https://doi.org/10.1515/IJDHD.2000.1.3.125

Wajnrajch, M, Gertner, J, Mullis, P, Deladoey, J, Cogan, J, Lekhakula, S, Kim, S, Dannies, P, Saenger, P, Moshang, T, Phillips III, J, Leibel, R. Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene. International Journal on Disability and Human Development. ;1(3): 125-136. https://doi.org/10.1515/IJDHD.2000.1.3.125

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CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.2000.1.3.125

Artikel in diesem Heft

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR