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

M. Lessi,; M. Giordano,; R. Paracchini,; A. Petri,; G. Federico,; M. Wasniewska,; A.M. Pasquino,; G. Aimaretti,; G. Bona,; P. Momigliano-Richiardi,

doi:10.1515/IJDHD.2001.2.4.215

Startseite 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

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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

M. Lessi, , M. Giordano, , R. Paracchini, , A. Petri, , G. Federico, , M. Wasniewska, , A.M. Pasquino, , G. Aimaretti, , G. Bona, und P. Momigliano-Richiardi,

Veröffentlicht/Copyright: 1. Oktober 2001

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Aus der Zeitschrift International Journal on Disability and Human Development Band 2 Heft 4

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Lessi,, M., Giordano,, M., Paracchini,, R., Petri,, A., Federico,, G., Wasniewska,, M., Pasquino,, A.M., Aimaretti,, G., Bona,, G. and Momigliano-Richiardi,, P.. "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" International Journal on Disability and Human Development, vol. 2, no. 4, pp. 215-228. https://doi.org/10.1515/IJDHD.2001.2.4.215

Lessi,, M., Giordano,, M., Paracchini,, R., Petri,, A., Federico,, G., Wasniewska,, M., Pasquino,, A., Aimaretti,, G., Bona,, G. & Momigliano-Richiardi,, P. (). 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. International Journal on Disability and Human Development, 2(4), 215-228. https://doi.org/10.1515/IJDHD.2001.2.4.215

Lessi,, M., Giordano,, M., Paracchini,, R., Petri,, A., Federico,, G., Wasniewska,, M., Pasquino,, A., Aimaretti,, G., Bona,, G. and Momigliano-Richiardi,, P. () 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. International Journal on Disability and Human Development, Vol. 2 (Issue 4), pp. 215-228. https://doi.org/10.1515/IJDHD.2001.2.4.215

Lessi,, M., Giordano,, M., Paracchini,, R., Petri,, A., Federico,, G., Wasniewska,, M., Pasquino,, A.M., Aimaretti,, G., Bona,, G. and Momigliano-Richiardi,, P.. "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" International Journal on Disability and Human Development 2, no. 4 (): 215-228. https://doi.org/10.1515/IJDHD.2001.2.4.215

Lessi, M, Giordano, M, Paracchini, R, Petri, A, Federico, G, Wasniewska, M, Pasquino, A, Aimaretti, G, Bona, G, Momigliano-Richiardi, P. 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. International Journal on Disability and Human Development. ;2(4): 215-228. https://doi.org/10.1515/IJDHD.2001.2.4.215

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Published Online: 2001-10

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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
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https://doi.org/10.1515/IJDHD.2001.2.4.215

Artikel in diesem Heft

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