Add to ORKGThese authors contributed equally to this work. Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms °to whom correspondence should be addressed: Human Development and Health Academic Unit, Faculty of Medicine. University of Southampton, Tremona Road, Southampton, SO16 6YD, UK
<p>(A) Confirmation of recessive <i>NLRP7</i> mutations in female patients and heterozygous status i...
NOD-like receptor proteins (NLRPs) are emerging key players in several inflammatory pathways in Mamm...
Background: NLRP7 (NALP7) has recently been identified as the causative gene for familial recurrent ...
Human imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Human-imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Human-imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Background Genomic imprinting results from the resistance of germline epigenetic marks to reprogramm...
Genetic, and indeed genomic, imprinting does occur in humans. This is manifest at the level of the g...
Genomic imprinting results from the resistance of germline epigenetic marks to reprogramming in the ...
Background: Human reproductive issues affecting fetal and maternal health are caused by numerous exo...
Background: A subset of individuals affected by imprinting disorders displays multi-locus imprinting...
Background: NLRP7 mutations are responsible for recurrent molar pregnancies and associated reproduct...
NLRP7 is a maternal effect gene in humans whose mutations are responsible for a rare abnormal pregna...
Many imprinted genes are necessary for normal human development. Approximately 70 imprinted genes ha...
Background: Imprinting disorders are a group of congenital diseases which are characterized by molec...
<p>(A) Confirmation of recessive <i>NLRP7</i> mutations in female patients and heterozygous status i...
NOD-like receptor proteins (NLRPs) are emerging key players in several inflammatory pathways in Mamm...
Background: NLRP7 (NALP7) has recently been identified as the causative gene for familial recurrent ...
Human imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Human-imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Human-imprinting disorders are congenital disorders of growth, development and metabolism, associate...
Background Genomic imprinting results from the resistance of germline epigenetic marks to reprogramm...
Genetic, and indeed genomic, imprinting does occur in humans. This is manifest at the level of the g...
Genomic imprinting results from the resistance of germline epigenetic marks to reprogramming in the ...
Background: Human reproductive issues affecting fetal and maternal health are caused by numerous exo...
Background: A subset of individuals affected by imprinting disorders displays multi-locus imprinting...
Background: NLRP7 mutations are responsible for recurrent molar pregnancies and associated reproduct...
NLRP7 is a maternal effect gene in humans whose mutations are responsible for a rare abnormal pregna...
Many imprinted genes are necessary for normal human development. Approximately 70 imprinted genes ha...
Background: Imprinting disorders are a group of congenital diseases which are characterized by molec...
<p>(A) Confirmation of recessive <i>NLRP7</i> mutations in female patients and heterozygous status i...
NOD-like receptor proteins (NLRPs) are emerging key players in several inflammatory pathways in Mamm...
Background: NLRP7 (NALP7) has recently been identified as the causative gene for familial recurrent ...