Literature DB >> 9683597

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

A P Jackson1, D P McHale, D A Campbell, H Jafri, Y Rashid, J Mannan, G Karbani, P Corry, M I Levene, R F Mueller, A F Markham, N J Lench, C G Woods.   

Abstract

Primary (or "true") microcephaly is inherited as an autosomal recessive trait and is thought to be genetically heterogeneous. Using autozygosity mapping, we have identified a genetic locus (MCPH1) for primary microcephaly, at chromosome 8p22-pter, in two consanguineous families of Pakistani origin. Our results indicate that the gene lies within a 13-cM region between the markers D8S1824 and D8S1825 (maximum multipoint LOD score of 8.1 at D8S277). In addition, we have demonstrated the genetic heterogeneity of this condition by analyzing a total of nine consanguineous families with primary microcephaly.

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Year:  1998        PMID: 9683597      PMCID: PMC1377307          DOI: 10.1086/301966

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  16 in total

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