HUMAN GENETICS

 Human Genetics: Volume 110, Number 2, February 2002
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	Original Investigation
LA eng
AU Ester Rozenblum, Pia Vahteristo, Therese Sandberg,
   Jon Thor Bergthorsson, Kirsi Syrjakoski, Don Weaver,
   Karin Haraldsson, Hrefna Kristin Johannsdottir, Paula Vehmanen,
   Savita Nigam, Natalie Golberger, Christiane Robbins,
   Evgenia Pak, Amalia Dutra, Elizabeth Gillander,
   Dietrich A.Stephan, Joan Bailey-Wilson, Suh-Hang Hank Juo,
   Tommi Kainu, Adalgeir Arason, Rosa Bjork Barkardottir,
   Heli Nevanlinna, Ake Borg, Olli-P.Kallioniemi
TE A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer
   development: identification and characterization of candidate
   genes
PP 111-121
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LA eng
AU Bao-li Chang, Siqun L.Zheng, Gregory A.Hawkins, Sarah D.Isaacs,
   Kathy E.Wiley, Aubrey Turner, John D.Carpten, Eugene R.Bleecker,
   Patrick C.Walsh, Jeffrey M.Trent, Deborah A.Meyers,
   William B.Isaacs, Jianfeng Xu
TE Polymorphic GGC repeats in the androgen receptor gene are
   associated with hereditary and sporadic prostate cancer risk
PP 122-129
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LA eng
AU Michael D.Brown, Elena Starikovskaya, Olga Derbeneva,
   Seyed Hosseini, Jon C.Allen, Irina E.Mikhailovskaya,
   Rem I.Sukernik, Douglas C.Wallace
TE The role of mtDNA background in disease expression: a new
   primary LHON mutation associated with Western Eurasian
   haplogroupnJ
PP 130-138
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LA eng
AU D.J.G.Mackay, A.-M.Coupe, J.P.H.Shield, J.N.P.Storr, I.K.Temple,
   D.O.Robinson
TE Relaxation of imprinted expression of ZAC and HYMAI in a patient
   with transient neonatal diabetes mellitus
PP 139-144
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LA eng
AU Bodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson,
   Hafez Ghulam Abbas, Goeran Anneren, Agne Larsson, Claes Wadelius
TE Linkage analysis identifies the thyroglobulin gene region as a
   major locus for familial congenital hypothyroidism
PP 145-147
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LA eng
AU Chun-Fang Xu, Karen Lewis, Kathryn L.Cantone, Parveen Khan,
   Christine Donnelly, Nicola White, Nikki Crocker, Pete R.Boyd,
   Dmitri V.Zaykin, Ian J.Purvis
TE Effectiveness of computational methods in haplotype prediction
PP 148-156
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LA eng
AU Patric Schoen, Ken Tsuchiya, Didier Lenoir, Toshio Mochizuki,
   Cecile Guichard, Setsuo Takai, Amit K.Maiti, Hiroshi Nihei,
   Johan Weil, Takahiko Yokoyama, Patrice Bouvagnet
TE Identification, genomic organization, chromosomal mapping and
   mutation analysis of the human INV gene, the ortholog of a
   murine gene implicated in left-right axis development and
   biliary atresia
PP 157-165
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LA eng
AU Giles D.J.Watts, Kathy C.O'Briant, Phillip F.Chance
TE Evidence of a founder effect and refinement of the hereditary
   neuralgic amyotrophy (HNA) locus on 17q25 in American families
PP 166-172
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LA eng
AU Dongfeng Gu, Sandra D.O'Dell, Xiao-he Chen, George J.Miller,
   Ian N.M.Day
TE Evidence of multiple causal sites affecting weight in the
   IGF2-INS-TH region of human chromosomen11
PP 173-181
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LA eng
AU Marco Seri, Maria Savino, Domenico Bordo, Roberto Cusano,
   Bianca Rocca, Ilaria Meloni, Filomena Di Bari, Pasi A.Koivisto,
   Martino Bolognesi, Gian Marco Ghiggeri, Raffaele Landolfi,
   Carlo L.Balduini, Leopoldo Zelante, Roberto Ravazzolo,
   Alessandra Renieri, Anna Savoia
TE Epstein syndrome: another renal disorder with mutations in the
   nonmuscle myosin heavy chainn9 gene
PP 182-186
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LA eng
AU Ruth M.Brown, Rosie A.Head, Garry K.Brown
TE Pyruvate dehydrogenase E3 binding protein deficiency
PP 187-191
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LA eng
AU Akira Tsujimura, Masao Ota, Yoshihiko Katsuyama, Masaharu Sada,
   Hidenobu Miura, Kiyomi Matsumiya, Rieko Gotoh, Takeshi Nakatani,
   Akihiko Okuyama, Shiro Takahara
TE Susceptibility gene for non-obstructive azoospermia located near
   HLA-DR and -DQ loci in the HLA classnII region
PP 192-197
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	Short Report
LA eng
AU Brigitte Pakendorf, Bharti Morar, Larissa A.Tarskaia,
   Manfred Kayser, Himla Soodyall, Alexander Rodewald,
   Mark Stoneking
TE Y-chromosomal evidence for a strong reduction in male population
   size of Yakuts
PP 198-200
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	Letter to the Editors
LA eng
AU Aoi Nakano, Hajime Nakano, Katsumi Hanada, Kazuo Nomura,
   Jouni Uitto
TE ZNT4 gene is not responsible for acrodermatitis enteropathica in
   Japanese families
PP 201-202
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	Book Review
LA eng
AU Alexandra J.Murray
TE Genetics in Medicine (Sixth Edition)
PP 203-204
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LA eng
AU Peter S.Harper
TE C.R.Scriver, A.L.Beaudet, W.S.Sly, D.Valle (eds.), B.Childs,
   K.W.Kinzler, B.Vogelstein (associate eds.): Molecular and
   metabolic bases of inherited disease, 8th edition
PP 205-206
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