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Examples
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Regarding the Enhance Trial The Enhance study involved 720 patients with a rare form of inherited high cholesterol known as Heterozygous Familial Hypercholesterolemia (HeFH) that affects less than 0.2 percent of the population.
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Heterozygous protein C deficiency in humans is associated with an increased incidence of thrombosis, while complete deficiency is generally fatal at birth or shortly thereafter.
unknown title 2011
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Heterozygous mutations in the gene encoding the CHD (chromodomain helicase DNA-binding domain) member CHD7, an ATP-dependent chromatin remodeller homologous to the
Naturejobs - All Jobs Ruchi Bajpai 2010
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Appukuttan B, Han J, Ito Y, Ai C, et al. (2000) Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts.
PLoS ONE Alerts: New Articles Anna Matynia et al. 2010
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Heterozygous mice in which the Igf1 gene underwent targeted disruption were bred, maintained and genotyped as described
PLoS ONE Alerts: New Articles Hortensia Sanchez-Calderon et al. 2010
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Heterozygous carriers (horses that had received the mutated gene from only one of their parents, meaning the syndrome did not show) were detected in high frequency in families known for this trait, they said.
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Heterozygous females exhibited normal lymphoid development and were indistinguishable from normal control females (data not shown).
PLoS ONE Alerts: New Articles Tomoji Mashimo et al. 2010
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Lin L, Philibert P, Ferraz-de-Souza B, et al. Heterozygous missense mutations in steroidogenic factor 1 (SF1 / Ad4BP, NR5A1) are associated with 46, XY disorders of sex development with normal adrenal function.
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Coutant R, Mallet D, Lahlou N, et al. Heterozygous mutation of steroidogenic factor-1 in 46, XY subjects may mimic partial androgen insensitivity syndrome.
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Lin L, Philibert P, Ferraz-de-Souza B, et al. Heterozygous missense mutations in steroidogenic factor 1 (SF1 / Ad4BP, NR5A1) are associated with 46, XY disorders of sex development with normal adrenal function.
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