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Rosenbaum Stella
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http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_23/101093hmgddn261/authorship/9
http://hub.abes.fr/oup/periodical/humrep/1994/volume_9/issue_9/101093oxfordjournalshumrepa138772/authorship/6
http://hub.abes.fr/oup/periodical/molehr/2000/volume_6/issue_7/101093molehr67591/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1996/volume_5/issue_7/101093hmg571047/authorship/6
http://hub.abes.fr/oup/periodical/brainj/2000/volume_123/issue_6/101093brain12361229/authorship/7
http://hub.abes.fr/oup/periodical/hmg/1996/volume_5/issue_1/101093hmg51159/authorship/1
http://hub.abes.fr/oup/periodical/molehr/1996/volume_2/issue_1/101093molehr2160/authorship/6
http://hub.abes.fr/oup/periodical/humrep/1998/volume_13/issue_6/101093humrep1361472/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/2006/volume_45/issue_9/101021bi0522504/authorship/10
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Muscular dystrophy due to dysferlin deficiency in Libyan Jews
A Gene for Non-Syndromic Autosomal Dominant Progressive Postlingual Sensorineural Hearing Loss Maps to Chromosome 14q12-13
Genetics: Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and ΔF508 mutations
Diagnosing and preventing inherited diseases
X inactivation-specific transcript expression in mouse oocytes and zygotes
Mitochondrial processes are impaired in hereditary inclusion body myopathy
Obstetric outcome after RhD and Kell testing.
Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1
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