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5 in total

1. Microdissection of the fragile X region.

Authors: R N MacKinnon; M C Hirst; M V Bell; J E Watson; U Claussen; H J Ludecke; G Senger; B Horsthemke; K E Davies
Journal: Am J Hum Genet Date: 1990-08 Impact factor: 11.025

2. Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Authors: H J Smeets; H G Brunner; H H Ropers; B Wieringa
Journal: Hum Genet Date: 1989-10 Impact factor: 4.132

3. Cardiac involvement in congenital myotonic dystrophy.

Authors: H Forsberg; B O Olofsson; A Eriksson; S Andersson
Journal: Br Heart J Date: 1990-02

4. Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Authors: B Smeets; J Poddighe; H Brunner; H H Ropers; B Wieringa
Journal: Hum Genet Date: 1988-09 Impact factor: 4.132

5. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.

Authors: H Smeets; L Bachinski; M Coerwinkel; J Schepens; J Hoeijmakers; M van Duin; K H Grzeschik; C A Weber; P de Jong; M J Siciliano
Journal: Am J Hum Genet Date: 1990-03 Impact factor: 11.025

5 in total