HUMAN GENETICS

 Human Genetics: Volume 110, Number 1, January 2002
~
	Original Investigation
LA eng
AU J.Balciuniene, L.Emilsson, L.Oreland, U.Pettersson, E.E.Jazin
TE Investigation of the functional effect of monoamine oxidase
   polymorphisms in human brain
PP 1-7
$$
LA eng
AU Henry Brodaty, Philip Mitchell, Georgina Luscombe,
   John B.J.Kwok, Renee F.Badenhop, Rod McKenzie, Peter R.Schofield
TE Familial idiopathic basal ganglia calcification (Fahr's disease)
   without neurological, cognitive and psychiatric symptoms is not
   linked to the IBGC1 locus on chromosome 14q
PP 8-14
$$
LA eng
AU Luca Scapoli, Marcella Martinelli, Furio Pezzetti,
   Francesco Carinci, Maria Bodo, Mauro Tognon, Paolo Carinci
TE Linkage disequilibrium between GABRB3 gene and nonsyndromic
   familial cleft lip with or without cleft palate
PP 15-20
$$
LA eng
AU Rene Santer, Sebastian Groth, Martina Kinner, Anja Dombrowski,
   Gerard T.Berry, Johannes Brodehl, James V.Leonard, Shimon Moses,
   Svante Norgren, Flemming Skovby, Reinhard Schneppenheim,
   Beat Steinmann, Juergen Schaub
TE The mutation spectrum of the facilitative glucose transporter
   gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome
PP 21-29
$$
LA eng
AU Leah Yogev, Ronni Gamzu, Gedalia Paz, Sandra Kleiman,
   Amnon Botchan, Ron Hauser, Haim Yavetz
TE Rate of homologous chromosome bivalents in spermatocytes may
   predict completion of spermatogenesis in azoospermic men
PP 30-35
$$
LA eng
AU Vesa Juvonen, Satu-Maria Kulmala, Jaakko Ignatius,
   Maila Penttinen, Marja-Liisa Savontaus
TE Dissecting the epidemiology of a trinucleotide repeat disease -
   example of FRDA in Finland
PP 36-40
$$
LA eng
AU Aoi Nakano, Sheau-Chiou Chao, Leena Pulkkinen, Dedee Murrell,
   Leena Bruckner-Tuderman, Ellen Pfendner, Jouni Uitto
TE Laminin 5 mutations in junctional epidermolysis bullosa:
   molecular basis of Herlitz vs non-Herlitz phenotypes
PP 41-51
$$
LA eng
AU Tin Aung, Louise Ocaka, Neil D.Ebenezer, Alex G.Morris,
   Michael Krawczak, Dawn L.Thiselton, Christiane Alexander,
   Marcela Votruba, Glen Brice, Anne H.Child, Peter J.Francis,
   Roger A.Hitchings, Ordan J.Lehmann, Shomi S.Bhattacharya
TE A major marker for normal tension glaucoma: association with
   polymorphisms in the OPA1 gene
PP 52-56
$$
LA eng
AU Lung-An Hsu, Yu-Lin Ko, Kuang-Hung Hsu, Yu-Hsien Ko,
   Ying-Shiung Lee
TE Genetic variations in the cholesteryl ester transfer protein
   gene and high density lipoprotein cholesterol levels in
   Taiwanese Chinese
PP 57-63
$$
LA eng
AU Angelo Selicorni, Silvana Guerneri, Antonia Ratti,
   Antonio Pizzuti
TE Cytogenetic mapping of a novel locus for typenII Waardenburg
   syndrome
PP 64-67
$$
LA eng
AU Zigmund Luka, Roberto Cerone, John A.Phillips III,
   S.Harvey Mudd, Conrad Wagner
TE Mutations in human glycine N-methyltransferase give insights
   into its role in methionine metabolism
PP 68-74
$$
LA eng
AU Hiroshi Honda, Norio Miharu, Yoko Ohashi, Osamu Samura,
   Masayuki Kinutani, Tetsuaki Hara, Koso Ohama
TE Fetal gender determination in early pregnancy through
   qualitative and quantitative analysis of fetal DNA in maternal
   serum
PP 75-79
$$
LA eng
AU Atsushi Tajima, I-Hung Pan, Goonnapa Fucharoen, Supan Fucharoen,
   Masafumi Matsuo, Katsushi Tokunaga, Takeo Juji, Masanori Hayami,
   Keiichi Omoto, Satoshi Horai
TE Three major lineages of Asian Ynchromosomes: implications for
   the peopling of east and southeast Asia
PP 80-88
$$
LA eng
AU Teruhiko Ito, Hirofumi Yasue, Michihiro Yoshimura,
   Shota Nakamura, Masafumi Nakayama, Yukio Shimasaki,
   Eisaku Harada, Yuji Mizuno, Hiroaki Kawano, Hisao Ogawa
TE Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated
   with coronary artery spasm
PP 89-94
$$
	Short Report
LA eng
AU Sevtap Savas, Ben Frischhertz, Mary Z.Pelias, Mark A.Batzer,
   Prescott L.Deininger, Bronya J.B.Keats
TE The USH1C 216GrarrA mutation and the 9-repeat VNTR(t,t) allele
   are in complete linkage disequilibrium in the Acadian population
PP 95-97
$$
	Letter to the editors
LA eng
AU Brian J.Morris
TE Critique of "Chromosome 17 and the inducible nitric oxide
   synthase gene in human essential hypertension" by Rutherford et
   al., Human Genetics, published online September 2001
PP 98-99
$$
LA eng
AU Lyn R.Griffiths
TE Authors response to: Critique of "Chromosomen17 and inducible
   nitric oxide synthase gene in human essential hypertension" by
   Rutherford et al. in Human Genetics published on-line September
   2001
PP 100-103
$$
	Book Review
LA eng
AU Rudolf Happle
TE Ulrich R.Hengge, Beatrix Volc-Platzer (eds): The skin and gene
   therapy
PP 104
$$
LA eng
AU Frances Flinter
TE Joyce C.Harper, Joy D.A.Delhanty, Alan H.Handyside (eds):
   Preimplantation genetic diagnosis
PP 105-106
$$
	Acknowledgement to Referees
LA eng
TE Acknowledgement to Referees 2001
PP 107-110
$$