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Publication Date:
January 2001
ISSN:
2191-0367

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International Journal on Disability and Human Development

Official journal of the the National Institute of Child Health and Human Development in Israel

Editor-in-Chief: Merrick, Joav

Editorial Board Member: Brooks, Tony / Carmeli, Eli / Dalton, Arthur J / Davidson, Philip W / Galil, Ahron / Heller, Tamar / Huff, Marlene B. / Janicki, Matthew P. / Kerr, Mike / Levy, Howard B / Lindström, Bengt / Morad, Mohammed / Omar, Hatim A. / Prasher, Vee / Shek, Daniel T.L. / Sher, Leo / Stratakis, Constantine A / Postolache, Teodor T.

4 Issues per year

Increased IMPACT FACTOR 2011: 0.300

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Issues

Ahead of print >

Volume 12 (2013)

Volume 11 (2012)

Volume 10 (2011)

Volume 9 (2010)

Volume 8 (2009)

Volume 7 (2008)

Volume 6 (2007)

Volume 5 (2006)

Volume 4 (2005)

Volume 3 (2003)

Volume 2 (2001)

Volume 1 (2000)

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  4. Acute alcohol-induced impairment of cognitive functions: Past and present findings by Fillmore , Mark Τ
  5. An exploratory study of patient interventions and nutritional advice for patients with chronic obstructive pulmonary disease, living in the community by Dickinson, Jill

Issue 1 (Jan 2001), pp. 1 - 74

CONTENTS

Page I

Letter from the Editors

Page 1

Molecular Genetics of Familial Hyperparathyroidism

Villablanca , A. / Höög , A. / Larsson , C. / Teh , B.T.

Page 3

Mutational Analysis of the Estrogen Receptor Alpha Gene in Israeli Osteoporotic Men and Women

Eckstein , M. / Vered , I. / Karasik , A. / Shalom , S. Ish / Nobikov , I. / Weisman , Y. / Friedman , E.

Page 13

Somatic Mutation Analysis of the MEN1 Gene in Adrenocortical Tumors Using Denaturing Gradient Gel Electrophoresis (DGGE)

Mark , M. / Morelli , A. / Brandi , M.L. / Falchetti , A. / Olchovski , D. / Arnaldi , G. / Mantero , F. / Friedman , E.

Page 21

The Human Germ Cell-Less (HGCL): A Candidate Gene for Alström Syndrome

Nili , E. / Cojocaru , G.S. / Collin , G.B. / Nishina , P.M. / Brok-Simoni , F. / Amariglio , N. / Simon , A.J. / Rechavi , G.

Page 29

Clinical, Hormonal and Molecular Genetic Characterization of Hungarian Patients with 11β-Hydroxylase Deficiency

Solyom , J. / Racz , K. / Peter , F. / Homoki , J. / Sippell , W.G. / Peter , M.

Page 37

Molecular Analysis of the Growth Hormone Gene (GH1) in Isolated Growth Hormone Deficiency

Giordano , M. / Lessi , M. / Paracchini , R. / Petri , A. / Ozerkan , E. / Cavallo , L. / Wasniewska , M. / Aimaretti , G. / Momigliano-Richiardi , P. / Bona , G.

Page 45

A Novel Polymorphism in Exon 4 of the Growth Hormone Gene and Association of Short Stature with a Known 5' UTR Polymorphism

Counts , D. / Palese , T.

Page 55

Complete Deficiency of Growth Hormone, Thyrotropin and Prolactin in Two Siblings: A New Pit-1 Mutation

Bircan , İ. / Semiz , S. / Cogan , J.D. / Hedges , L.K.

Page 61

BOOK REVIEWS. CALENDAR

Page 69

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