Use of linkage data obtained in single families: Prenatal diagnosis of a new X-linked mental retardation syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference18 articles.
1. Report of the committee on methods of linkage analysis and reporting
2. Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
3. The Genetic Linkage Map of the Human X Chromosome
4. (1992) Characterisation of new PCR markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci. Am J Med Genet, this issue.
5. Report of the committee on clinical disorders and chromosomal deletion syndromes
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy;Nature Genetics;1995-10
2. Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28;American Journal of Medical Genetics;1993-02-01
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