Results 131 to 140 of about 40,494 (265)
Parental violent offending and offspring suicidal behavior: a nationwide register-based study. [PDF]
Järvinen A +8 more
europepmc +1 more source
Abstract Myotonic dystrophy type 1 (DM1) is a clinically challenging multisystem neuromuscular hereditary disorder, with generational increase in severity and earlier age at onset. It is caused by an unstable cytosine‐thymine‐guanine repeat expansion at the DMPK locus, accompanied by associated genetic and epigenetic modifications.
Md Mehedi Hasan +9 more
wiley +1 more source
Editorial: Plasticity and flexibility in the parental brain
Natalia Uriarte, Mariana Pereira
doaj +1 more source
Parental differential treatment and symptoms of child psychopathology: A twin study. [PDF]
Maravilla JP +4 more
europepmc +1 more source
Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
ABSTRACT Objective In‐utero cell and gene therapies may offer prenatal treatment options for inherited diseases. Preclinical data suggests in‐utero (IU) hematopoietic stem cell transplantation (HSCT) could prevent Fanconi anemia (FA) related bone marrow failure without genotoxic conditioning or immune suppression.
Tony Lum +4 more
wiley +1 more source
How do male partners experience the pre- and postpartum period depending on maternal anorexia nervosa? Findings from a qualitative interview study. [PDF]
Throm JK +4 more
europepmc +1 more source
Partible paternity and human reproductive behavior
Partible paternity refers to the concept that children can have more than one father. The theory and practice of partible paternity appears exclusive to South America, where it is common among indigenous societies of Amazonia. Such an outlook on reproduction is accompanied by patterns of polygynandrous mating, and has generated cultural institutions ...
openaire +2 more sources
ABSTRACT Objective Prenatal genetic testing for imprinting disorders is rarely requested with the exception of Beckwith‐Wiedemann syndrome (BWS) which is associated with specific ultrasound findings (e.g., placental mesenchymal dysplasia, omphalocele). However, genetic testing for BWS is challenging as aberrant DNA methylation has to be addressed which
Melissa Connolly +10 more
wiley +1 more source
Regulatory role of prolactin in paternal behavior in male parents: A narrative review.
Hashemian F, Shafigh F, Roohi E.
europepmc +1 more source
ABSTRACT Objectives Partial gene duplications (PGDups) are a significant contributor to genetic disease. The precise genomic location and structure of PGDups are often unresolved using conventional methods, so prenatal diagnosis for PGDups is challenging, especially without ultrasound abnormalities.
Shengfang Qin +10 more
wiley +1 more source

