Chromosome Disorders (metabolism) < Chromosome Mapping < Chromosome Mapping (methods)

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List of bibliographic references

Number of relevant bibliographic references: 37.
[20-40] [0 - 20][0 - 37]

Ident.	Authors (with country if any)	Title
001713 (2006)	Shaochun Ma [États-Unis] ; Thomas L. Davis ; Marcia A. Blair ; John Y. Fang ; Yuki Bradford ; Jonathan L. Haines ; Peter Hedera	Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
001A87 (2007)	Fabin Han [Canada] ; Lemuel Racacho ; Anthony E. Lang ; Dennis E. Bulman ; David A. Grimes	Refinement of the DYT15 locus in myoclonus dystonia.
001B03 (2007)	Claudia Cagnoli ; Alessandro Brussino ; Eleonora Di Gregorio ; Alfredo Brusco ; Giovanni Stevanin ; Alexandra Durr ; Alexis Brice	The (-16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients.
001B09 (2007)	Christoph Kamm [Allemagne] ; Petra Mayer ; Manu Sharma ; Gerhard Niemann ; Thomas Gasser	New family with paroxysmal exercise-induced dystonia and epilepsy.
001B22 (2007)	Hiroaki Nozaki [Japon] ; Takeshi Ikeuchi ; Akio Kawakami ; Akio Kimura ; Reiji Koide ; Miyuki Tsuchiya ; Yuusaku Nakmura ; Tatsuro Mutoh ; Hiroko Yamamoto ; Naoki Nakao ; Ko Sahashi ; Masatoyo Nishizawa ; Osamu Onodera	Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
001B40 (2007)	Deborah A. Hall [États-Unis] ; Julie Parsons ; Tim Benke	Paroxysmal nonkinesigenic dystonia and celiac disease.
002080 (2008)	Hiltrud Muhle [Allemagne] ; Anja Neumann ; Katja Lohmann-Hedrich ; Thora Lohnau ; Yang Lu ; Susen Winkler ; Stephan Waltz ; Anke Fischenbeck ; Patricia L. Kramer ; Christine Klein ; Ulrich Stephani	Childhood-onset restless legs syndrome: clinical and genetic features of 22 families.
002329 (2008)	Maria G. Motlagh [États-Unis, Iran] ; Arshia Seddigh [Iran, Royaume-Uni] ; Behnoosh Dashti [Iran] ; James F. Leckman [États-Unis] ; Javad Alaghband-Rad [Iran, Canada]	Consanguineous Iranian Kindreds with Severe Tourette Syndrome
002D12 (2010)	Antonetta M G. Sas [Pays-Bas] ; Alessio Di Fonzo ; Stef L M. Bakker ; Erik J. Simons ; Ben A. Oostra ; Anneke J. Maat-Kievit ; Agnita J W. Boon ; Vincenzo Bonifati	Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
003816 (2012)	Jessie Theuns [Belgique] ; David Crosiers ; Luc Debaene ; Karen Nuytemans ; Bram Meeus ; Kristel Sleegers ; Dirk Goossens ; Ellen Corsmit ; Ellen Elinck ; Karin Peeters ; Maria Mattheijssens ; Barbara Pickut ; Jurgen Del-Favero ; Sebastiaan Engelborghs ; Peter Paul De Deyn ; Patrick Cras ; Christine Van Broeckhoven	Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.
004204 (2015)	Janel O. Johnson [Royaume-Uni] ; Giovanni Stevanin ; Joyce Van De Leemput ; Dena G. Hernandez ; Sampath Arepalli ; Sylvie Forlani ; Reza Zonozi ; J Raphael Gibbs ; Alexis Brice ; Alexandra Durr ; Andrew B. Singleton	A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.
004772 (1994)	S B Bressman [États-Unis] ; A L Hunt ; G A Heiman ; M F Brin ; R E Burke ; S. Fahn ; J M Trugman ; D. De Leon ; P L Kramer ; K C Wilhelmsen	Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.
004813 (1994)	V. Planté-Bordeneuve [Royaume-Uni] ; M B Davis ; D M Maraganore ; C D Marsden ; A E Harding	Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease.
004A76 (1996)	T. Gasser [États-Unis] ; C M Bove ; L J Ozelius ; M. Hallett ; M E Charness ; F H Hochberg ; X O Breakefield	Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.
004B65 (1996)	T. Gasser [Allemagne] ; B. Bereznai ; B. Müller ; R. Pruszak-Seel ; R. Damrich ; G. Deuschl ; W H Oertel	Linkage studies in alcohol-responsive myoclonic dystonia.
004F34 (1998)	R C Duvoisin [États-Unis]	Role of genetics in the cause of Parkinson's disease.
005082 (1998)	S L Ho [Hong Kong] ; M H Kung	G209A mutation in the alpha-synuclein gene is rare and not associated with sporadic Parkinson's disease.

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