Human Genetics,volume 110,issue 2  (02-2002)

Period of time: 2002年2期

Publisher: Springer Publishing Company

Founded in: 1913

Total resources: 46

ISSN: 0340-6717

Subject: Q3 Genetics

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Human Genetics,volume 110,issue 2

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A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

By Rozenblum Ester,Vahteristo Pia,Sandberg Therese,Bergthorsson Jon,Syrjakoski Kirsi,Weaver Don,Haraldsson Karin,Johannsdottir Hrefna,Vehmanen Paula,Nigam Savita,Golberger Natalie,Robbins Christiane,Pak Evgenia,Dutra Amalia,Gillander Elizabeth,Stephan Dietrich,Bailey-Wilson Joan,Juo Suh-Hang,Kainu Tommi,Arason Adalgeir,Barkardottir Rosa,Nevanlinna Heli,Borg Ake,Kallioniemi Olli-P. in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 111-121

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Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk

By Chang Bao-li,Zheng Siqun,Hawkins Gregory,Isaacs Sarah,Wiley Kathy,Turner Aubrey,Carpten John,Bleecker Eugene,Walsh Patrick,Trent Jeffrey,Meyers Deborah,Isaacs William,Xu Jianfeng in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 122-129

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

By Brown Michael,Starikovskaya Elena,Derbeneva Olga,Hosseini Seyed,Allen Jon,Mikhailovskaya Irina,Sukernik Rem,Wallace Douglas in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 130-138

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Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism

By Ahlbom Bodil,Yaqoob Muhammad,Gustavsson Peter,Abbas Hafez,Annerén Göran,Larsson Agne,Wadelius Claes in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 145-147

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Effectiveness of computational methods in haplotype prediction

By Xu Chun-Fang,Lewis Karen,Cantone Kathryn,Khan Parveen,Donnelly Christine,White Nicola,Crocker Nikki,Boyd Pete,Zaykin Dmitri,Purvis Ian in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 148-156

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Identification, genomic organization, chromosomal mapping and mutation analysis of the human gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia

By Schön Patric,Tsuchiya Ken,Lenoir Didier,Mochizuki Toshio,Guichard Cécile,Takai Setsuo,Maiti Amit,Nihei Hiroshi,Weil Johan,Yokoyama Takahiko,Bouvagnet Patrice in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 157-165

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Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

By Seri Marco,Savino Maria,Bordo Domenico,Cusano Roberto,Rocca Bianca,Meloni Ilaria,Bari Filomena,Koivisto Pasi,Bolognesi Martino,Ghiggeri Gian,Landolfi Raffaele,Balduini Carlo,Zelante Leopoldo,Ravazzolo Roberto,Renieri Alessandra,Savoia Anna in (2002)

Human Genetics,volume 110,issue 2 , Vol. 110, Iss. 2, 2002-02 , pp. 182-186

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