Literature DB >> 2858726

Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.

I Oberlé, J L Mandel, J Boué, M G Mattei, J F Mattei.   

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Year:  1985        PMID： 2858726     DOI： 10.1016/s0140-6736(85)92228-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 in total

1.  A new MspI restriction fragment length polymorphism in the hemophilia B locus.

Authors:  G Camerino; I Oberlé; D Drayna; J L Mandel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Multilocus analysis of the fragile X syndrome.

Authors:  W T Brown; A Gross; C Chan; E C Jenkins; J L Mandel; I Oberlé; B Arveiler; G Novelli; S Thibodeau; R Hagerman
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

3.  Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features.

Authors:  J C Mixon; V G Dev
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

4.  The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis.

Authors:  M G Butler; V G Dev; D Shah; J E Ulm; P L Wilmot; L R Shapiro
Journal:  Am J Med Genet       Date:  1988-12
  4 in total

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