Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04149.x/fullpdf
Reference34 articles.
1. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome;Ballabio;Proc Natl Acad Sci USA,1989
2. Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region;Ballabio;Genomics,1990
3. Isolation and characterisation of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis;Ballabio;Proc Natl Acad Sci USA,1987
4. Brief clinical report: neural tube defects as an X-linked condition;Baraitser;Am J Med Genet,1984
5. The embryonic development of mammalian neural tube defects;Copp;Prog Neurobiol,1990
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