نتائج البحث

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.

• Authors : Kember, Rachel L.¹; Georgi, Benjamin¹; Bailey-Wilson, Joan E.²

Subjects: *DNA copy number variations; *GENETICS of bipolar disorder; *AFFECTIVE disorders

• Source: BMC Genetics. 2015, Vol. 16 Issue 1, preceding p2-15. 16p.

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.

• Authors : Brooks P; IntegraGen SA, Evry, France. ; Marcaillou C

Subjects: Phenotype*; Chromosome Mapping/Chromosome Mapping/Chromosome Mapping/*methods ; Collagen/Collagen/Collagen/*genetics

• Source: BMC genetics [BMC Genet] 2009 Mar 30; Vol. 10, pp. 16. Date of Electronic Publication: 2009 Mar 30.Publisher: BioMed Central Country of Publication: England NLM ID: 100966978 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2156

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta

• Authors : Cohen Nadine; Favis Reyna; Francke Stephan

Subjects: Genetics; QH426-470

• Source: BMC Genetics, Vol 10, Iss 1, p 16 (2009)

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Homozygosity by descent mapping of blood pressure in the Old Order Amish: evidence for sex specific genetic architecture.

• Authors : McArdle PF; Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA. ; Dytch H

Subjects: Chromosome Mapping* ; Genetic Predisposition to Disease* ; Homozygote*

• Source: BMC genetics [BMC Genet] 2007 Oct 01; Vol. 8, pp. 66. Date of Electronic Publication: 2007 Oct 01.Publisher: BioMed Central Country of Publication: England NLM ID: 100966978 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2156

تفاصيل العنوان

Homozygosity by descent mapping of blood pressure in the OldOrder Amish: evidence for sex specific genetic architecture.

• Source: BMC Genetics. 2007, Vol. 8, p66-74. 9p.

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta

• Authors : Frédéric Tores; Nadine Cohen; Peter Brooks

Subjects: Genetic Markers; lcsh:QH426-470; DNA Mutational Analysis

• Source: BMC Genetics, Vol 10, Iss 1, p 16 (2009)BMC Genetics

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