Results 41 to 50 of about 16,399 (267)

The problems of determining the competence of the subjects of the Russian Federation in the field of family protection

Правоприменение, 2017
УДК 342This article is dedicated to one of the problematic issues of Russian federalism – the definition of the competence of subjects of the Russian Federation in the social sphere related to the protection of the family.Results.
S. Narutto
doaj   +1 more source

The Position of Genetic Father under Turkish Paternity Law

İstanbul Hukuk Mecmuası, 2022
As in many legal systems, the establishment of a legal paternal relationship between a father and a child under TurkishSwiss law is not directly based on genetic lineage.
Şirin Aydıncık Midyat
doaj   +1 more source

A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco, Aaron Williams, Claudia Soler‐Alfonso, Emily Waskow, Elizabeth Mizerik, Fernando Scaglia, Chaya N. Murali   +6 more
wiley   +1 more source

‘Seeking for clarity in genetic science’: exploring the factors behind men’s decisions to seek DNA testing in Zimbabwe

Cogent Social Sciences
The study investigates factors that influence men’s decisions to seek deoxyribonucleic acid (DNA) paternity tests in Zimbabwe. A qualitative descriptive phenomenological design was used as a research design.
Zvikomborero M. Robson, Charles Simbarashe Gozho, Taruvinga Muzingili   +2 more
doaj   +1 more source

Severe ADEM‐Like Neuroinflammatory Disease and Cerebrovascular Fragility With Recurrent Pseudoaneurysms and Moyamoya in a Familial Germline CBL Mutation: Expanding the Clinical Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous germline variants in CBL disrupt its function as a negative regulator of the Ras/MAPK pathway, classically predisposing to Juvenile myelomonocytic leukemia (JMML) and moyamoya. We describe two affected siblings carrying a paternally inherited CBL variant (c.1210 T> C, p.
Michal Bar‐Hakim, Anat Abramovich, Sara Via‐Dorembus, Gali Heimer, Bruria Ben‐Zeev, Etai Adam, Assaf A. Barg, Jonathan Roth, Basheer Sheick‐Yousif, Rony Beeri Berkowiz, Michal Feldon, Haim Bassan, Moran Hausman‐Kedem   +12 more
wiley   +1 more source

PATERNITY LEAVE (CUTI AYAH): Apa, Bagaimana dan untuk Apa?

Yinyang: Jurnal Studi Islam, Gender dan Anak, 2017
: Paternity leave is part of the parental leave program. Paternity leave is a leave policy given to male workers by many reason, when childbirth or adopting a child. Paternity leave is essential for reconciling work and family life for men.
Dewi Ariyani
doaj  

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert, Gudny Anna Arnadottir, Laura Bedinger, Nicola Brunetti‐Pierri, Jennifer Cech, Xin Chen, Yanmin Chen, Erika Chick, Sarah Dyack, Madeleine Franchi, Tanja Frey, David Genevieve, Ian Glass, Jorge Granadillo, Kelly A. Keener, Sara B. MacKay, Paige McDunnah, Vinod K. Misra, Kristin G. Monaghan, Sureni V. Mullegama, Cristina Peduto, Leia Peterman‐Prather, Anita Rauch, Cherith Somerville, Kari Stefansson, Katharina Steindl, Patrick Sulem, Telma Sulem, Pamela Trapane, Roberta Zeuli, Samuel Zinner, Kosuke Izumi   +31 more
wiley   +1 more source

Ser pai no subúrbio ferroviário de Salvador: um estudo de caso com homens de camadas populares Being a father in the railroad suburb of Salvador: a study case with men from popular classes

Psicologia em Estudo, 2005
Realizamos um estudo de cunho etnográfico com homens de camadas populares, pais de crianças menores de seis anos, procurando conhecer suas vivências em torno da paternidade e estabelecendo nexos com discursos e práticas.
Vânia Bustamante
doaj   +1 more source

High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops‐Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nonimmune hydrops fetalis (NIHF) is characterized by abnormal fluid accumulation in ≥ 2 fetal compartments and may be genetic. The incremental diagnostic yield of prenatal exome sequencing (ES) for NIHF following a negative standard workup was previously explored on 22 cases.
Stephanie M. Rice, Mona M. Makhamreh, Sascha Wodoslawsky, Mariella Toro, Elizabeth Critchlow, Brandy Firman, Ruby Liu, Babi Ramesh Nallamilli, Madhuri Hegde, Seth I. Berger, Huda B. Al‐Kouatly   +10 more
wiley   +1 more source

Microsatellite Primers for Parkia biglobosa (Fabaceae: Mimosoideae) Reveal that a Single Plant Sires All Seeds Per Pod

Applications in Plant Sciences, 2014
Premise of the study: Microsatellite primers were developed for an indigenous fruit tree, Parkia biglobosa, as a tool to study reproductive biology and population structure. Here we use the primers to determine the number of fathers per pod. Methods and
Kristin Marie Lassen, Erik Dahl Kjær, Moussa Ouédraogo, Lene Rostgaard Nielsen   +3 more
doaj   +1 more source