SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly - Concepedia

Concepedia

Publication | Closed Access

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

73

Citations

22

References

2005

Year

Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Farkhondeh Behjati, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saghar Ghasemi Firouzabadi, Christian Becker, Franz Rüschendorf, Peter Nürnberg,

Developmental BiologyMendelian DisorderBrain DevelopmentGenetic DisorderGeneticsPsychiatric GeneticsMedical GeneticsMedicineMild MicrocephalyNeurogenetics

References

	Year	Citations

Page 1

Page 1