Results 111 to 120 of about 1,676,195 (294)

Pregnancy discrimination in the workplace: legal framework and review of legal decisions 1999 to 2008

open access: yes, 2011
The experience of being in employment while pregnant or returning to work after having a child is not well researched in Ireland or indeed internationally.
Russell, Helen, Banks, Joanne
core  

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

open access: yesAmerican 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   +10 more
wiley   +1 more source

Concealed pregnancy: a case-study approach from an Irish setting

open access: yes, 2006
This study arose out of interested and concerned observations of social work and crisis pregnancy counselling and support staff attached to the antenatal and maternity departments of an Irish rural-based general hospital.
Conlon, Catherine
core  

Screening for domestic violence during pregnancy: options for future reporting in the National Perinatal Data Collection [PDF]

open access: yes, 2015
This report discusses barriers to, and opportunities for, the collection of data on screening for domestic violence during pregnancy. Summary Domestic violence (DV), defined in this paper as \u27acts of violence that occur between people who have, or ...
Australian Institute of Health and Welfare
core  

An Adult Presentation of KIF11‐Related MCLID Syndrome: Case Report and 40‐Year Follow‐Up

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in KIF11 are linked to autosomal dominant syndromes with microcephaly, chorioretinopathy, lymphedema, and intellectual disability (MCLID), though adult presentations remain underreported. We report a 42‐year‐old female presenting with a de novo single‐amino acid in‐frame deletion in the KIF11 gene (c.1294_1296del; p ...
Thrishna Chathurvedula   +8 more
wiley   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright   +10 more
wiley   +1 more source

Literature review on provision of appropriate and accessible support to people with an intellectual disability who are experiencing crisis pregnancy

open access: yes, 2011
The Crisis Pregnancy Agency [2] and the National Disability Authority commissioned this systematic review of Irish and international literature to identify international models of good practice regarding crisis pregnancy counselling and support ...
O'Connor, Joan
core  

Home - About - Disclaimer - Privacy