Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.

Paternal but not maternal age influences early-life performance of offspring in a long-lived seabird.

Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.

Molecular mechanisms leading to the phenotypic development in paternal and maternal uniparental disomy for chromosome 14.

Maternal and paternal contribution to intergenerational psychosocial transmission of paan chewing.

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

Obesity Leads to Tissue, but not Serum Vitamin A Deficiency.

Angelman syndrome.

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Angelman syndrome in adulthood.

Neurodevelopmental Underpinnings of Angelman Syndrome.

Angelman syndrome: clinical profile.

Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model.

Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice.

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

Diagnostic approach of angelman syndrome.

Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age.

Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia.

Differential Expression of Ecdysone Receptor Leads to Variation in Phenotypic Plasticity across Serial Homologs.

Angelman Syndrome: A Case Report.

Hypotonic treatment leads to chromosomal aberrations but not to sister-chromatid exchanges in human lymphocytes.

Neural control of maternal and paternal behaviors.

Maternal transmission of translocation 2;21 associated with Down's syndrome.

Paroxysmal tonic upward gaze complicating Angelman syndrome.

Pro-social 50-kHz ultrasonic communication in rats: post-weaning but not post-adolescent social isolation leads to social impairments-phenotypic rescue by re-socialization.

Suggest Documents

Paternal but not maternal age influences early-life performance of offspring in a long-lived seabird.

Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.

Molecular mechanisms leading to the phenotypic development in paternal and maternal uniparental disomy for chromosome 14.

Maternal and paternal contribution to intergenerational psychosocial transmission of paan chewing.

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

Obesity Leads to Tissue, but not Serum Vitamin A Deficiency.

Angelman syndrome.

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Angelman syndrome in adulthood.

Neurodevelopmental Underpinnings of Angelman Syndrome.

Angelman syndrome: clinical profile.

Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model.

Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice.

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

Diagnostic approach of angelman syndrome.

Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age.

Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia.

Differential Expression of Ecdysone Receptor Leads to Variation in Phenotypic Plasticity across Serial Homologs.

Angelman Syndrome: A Case Report.

Hypotonic treatment leads to chromosomal aberrations but not to sister-chromatid exchanges in human lymphocytes.

Neural control of maternal and paternal behaviors.

Maternal transmission of translocation 2;21 associated with Down's syndrome.

Paroxysmal tonic upward gaze complicating Angelman syndrome.

Pro-social 50-kHz ultrasonic communication in rats: post-weaning but not post-adolescent social isolation leads to social impairments-phenotypic rescue by re-socialization.

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.

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