Literature DB >> 3808324

Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele.

R J Bartlett, M A Pericak-Vance, J T Lanman, A P Killam, J R Gilbert, J M Stajick, J C Chen, T Siddique, R S Kandt, M Sirotkin-Roses.   

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Year:  1987        PMID： 3808324     DOI： 10.1212/wnl.37.2.355

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

Review 1.  Investigation of muscle disease.

Authors:  F L Mastaglia; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-03       Impact factor: 10.154

2.  Familial inheritance of a DXS164 deletion mutation from a heterozygous female.

Authors:  J T Lanman; M A Pericak-Vance; R J Bartlett; J C Chen; L Yamaoka; J Koh; M C Speer; W Y Hung; A D Roses
Journal:  Am J Hum Genet       Date:  1987-08       Impact factor: 11.025

3.  Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.

Authors:  N G Laing; P A Akkari; D C Chandler; H E Thomas; M G Layton; M E Mears; B A Kakulas
Journal:  Nucleic Acids Res       Date:  1990-07-25       Impact factor: 16.971
  3 in total

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