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Beckmann J. S.
Beckmann Jacques
Beckmann Jacques S.
Beckmann J.S.
Beckmann J.
S.Beckmann Jacques
Beckmann Jacques S
Beckmann J S
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http://hub.abes.fr/bmj/periodical/jmedgenet/1994/volume_31/issue_4/B35966E222856AB5E053120B220AFD24/authorship/10
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_5/B3598D6B5C467CBEE053120B220A90C5/authorship/11
http://hub.abes.fr/bmj/periodical/jmg/2012/volume_49/issue_10/B35958AFB0386AAFE053120B220A26C8/authorship/3
http://hub.abes.fr/oup/periodical/nar/1992/volume_20/issue_5/101093nar2051166/authorship/4
http://hub.abes.fr/oup/periodical/bioinformatics/2005/volume_21/issue_16/101093bioinformaticsbti537/authorship/6
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http://hub.abes.fr/oup/periodical/brainj/2000/volume_123/issue_6/101093brain12361229/authorship/9
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_12/101093hmg3122269/authorship/9
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http://hub.abes.fr/oup/periodical/brainj/1998/volume_121/issue_9/101093brain12191735/authorship/12
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http://hub.abes.fr/oup/periodical/brainj/1996/volume_119/issue_1/101093brain1191295/authorship/11
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http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_12/101093hmg2122019/authorship/1
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_12/101093hmg2122199a/authorship/3
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http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_11/101093hmg4112155/authorship/6
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_9/101093hmg691401/authorship/5
http://hub.abes.fr/oup/periodical/brimed/1999/volume_55/issue_2/1012580007142991902411/authorship/1
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_1/101093hmg1164a/authorship/4
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http://hub.abes.fr/oup/periodical/nar/2008/volume_36/issue_21/101093nargkn812/authorship/6
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_2/101093hmg32382/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_5/101093hmg85855/authorship/14
http://hub.abes.fr/oup/periodical/nar/1992/volume_20/issue_5/101093nar2051166a/authorship/4
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http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_2/101093hmg32382a/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_2/101093hmg92165/authorship/11
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_9/101093hmg291423/authorship/3
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_3/101093hmg43459/authorship/10
http://hub.abes.fr/oup/periodical/hmg/1996/volume_5/issue_12/101093hmg5122019/authorship/13
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_4/101093hmg44717/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_3/101093hmg83409/authorship/6
http://hub.abes.fr/oup/periodical/nar/1992/volume_20/issue_5/101093nar2051165a/authorship/4
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of
Isolation of methotrexate-resistant cell lines in Petunia hybrida upon stepwise selection procedure
Elevated amounts of methotrexate-binding protein, different from normal dihydrofolate reductase, in a petunia MTXR-cell line
Physiology and genetics of carbamoylphosphate synthesis in Escherichia coli K12
Dinucleotide repeat polymorphism at the human Poly (ADP-Ribose) polymerase gene (PPOL)
A new minisatellite probe shows highly polymorphic hybridization pattern in human
A Founder Mutation in the γ-Sarcoglycan Gene of Gypsies Possibly Predating Their Migration Out of India
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes
Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations
Juvenile limb-girdle muscular dystrophy
Muscular dystrophy due to dysferlin deficiency in Libyan Jews
Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1)
A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus
An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites
Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus
FoldIndex©: a simple tool to predict whether a given protein sequence is intrinsically unfolded
Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin
Dinucleotide repeat at the D15S129 locus
Three dinucleotide markers on chromosome 21
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy
A Susceptibility Locus for Early-Onset Non-Insulin Dependent (Type 2) Diabetes Mellitus Maps to Chromosome 20q, Proximal to the Phosphoenolpyruvate Carboxykinase Gene
Disease taxonomy - monogenic muscular dystrophy
Isolation and nucleotide sequence of a plant tRNA gene: petunia asparagine tRNA
Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain).
Adhalin gene polymorphism
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