Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://www.springerlink.com/index/pdf/10.1007/BF00962557
Reference36 articles.
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2. Bennett M, Variend S, Pollitt R (1986) Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant death.Lancet 1470.
3. Bennett M, Allison F, Pollitt R, Manning N, Gray R, Green A, Hale D, Coates PM (1987) Prenatal diagnosis of medium-chain acyl CoA dehydrogenase deficiency in a family with sudden infant death.Lancet 1:440.
4. Bergman A, Beckwith J, Ray C (1970)Sudden Infant Death Syndrome. Seattle: University of Washington Press.
5. Carpenter R, Gardner A, Harris J, Judd M, Lewry J, Maddock CR, Powell J, Taylor EM (1988)Ann NY Acad Sci 533:96?103.
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