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Healthy Parent sentence examples within Consanguineou Healthy Parent

A case of transient hyperphosphatasemia presenting with mild degree of bow legs

A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review

Healthy Parent sentence examples within Unrelated Healthy Parent

Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia

The Wrath of Severe Term Hypoxic-Ischemic Encephalopathy

Healthy Parent sentence examples within Support Healthy Parent

Indigenous Mothers’ Use of Web- and App-Based Information Sources to Support Healthy Parenting and Infant Health in Canada: Interpretive Description

CenteringParenting - Forming a Community Inside the Medical Home through the Group Well Child Visit

Healthy Parent sentence examples within Periodontally Healthy Parent

Parents with periodontitis impact the subgingival colonization of their offspring

Dynamics of colonization by Aggregatibacter actinomycetemcomitans in aggressive periodontitis families

Healthy Parent sentence examples within Her Healthy Parent

SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia.

A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia

Healthy Parent sentence examples within Two Healthy Parent

Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A

A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 - Review of the literature.

Healthy Parent sentence examples within healthy parent carer

Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children

Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children.

Healthy Parent sentence examples within healthy parent feeding

Regulatory parental feeding behaviors, emotion suppression, and emotional eating in the absence of hunger: Examining parent-adolescent dyadic associations

Family functioning mediates the relationship between child behavior problems and parent feeding practices in youth with overweight or obesity.

Exome Sequencing Reveals De Novo Variants in Congenital Scoliosis

Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs

Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1A.

A new measure of excessive parental worries about children’s health: Development of the Health Anxiety by Proxy Scale (HAPYS)

A Novel Germline Compound Heterozygous Mutation of BRCA2 Gene Associated With Familial Peripheral Neuroblastic Tumors in Two Siblings

Parenting and Child Development: A Relational Health Perspective

Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain Reaction

Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets.

Child care institutions in India: Investigating issues and challenges in children’s rehabilitation and social integration

SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum

A Novel BLOC1S5-Related HPS-11 Patient and Zebrafish with bloc1s5 Disruption.

High-Throughput Screen Detects Calcium Signaling Dysfunction in Hutchinson-Gilford Progeria Syndrome

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Parenting in a Pandemic: An Innovative Virtual Support Forum for Families Living in Homeless Shelters

Potential impacts, alleviating factors, and interventions for children of a parent with schizophrenia: A scoping review

Autistic traits in offspring of schizophrenic patients in comparison to those of normal population: a case-control study

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Parenting skills of patients with chronic schizophrenia

Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy.

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

Promoting mother-infant relationships and underlying neural correlates: Results from a randomized controlled trial of a home-visiting program for adolescent mothers in Brazil.

Biased Maintenance of Attention on Sad Faces in Clinically Depressed Youth: An Eye-Tracking Study.

Tetrasomy 18p in one non-identical twin born to healthy parents: A case report

Barriers and facilitators to mood and confidence in pregnancy and early parenthood during COVID-19 in the UK: mixed-methods synthesis survey

Child Development and Well-Being


Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A).

Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors

Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies

The evaluation of depression, anxiety and quality of life in children living with parental cancer: A case-control study (eng)

Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant.

Mosaic trisomy 12 diagnosed in a female patient: clinical features, genetic analysis, and review of the literature

Newborns physiological differences in low- and high-altitude settings of Ecuador.

Loss of TANGO1 Leads to Absence of Bone Mineralization

Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios


Parenting in Patients with Borderline Personality Disorder, Sequelae for the Offspring and Approaches to Treatment and Prevention

A genome-wide CRISPR screen identifies N-acetylglucosamine-1-phosphate transferase as a potential antiviral target for Ebola virus

[Association between time-appropriate vaccinations in early childhood and individual and community-level factors in Japan].

[Relationship between pregnancy factors and low birth weight infants, miscarriages, and stillbirths: A follow-up survey on birth conditions of pregnant women who received the maternal and child health handbook from public health nurses and midwives].

CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.

Baseline and follow-up activity and functional connectivity in reward neural circuitries in offspring at risk for bipolar disorder

Comparison of attachment styles of addicted parents and non-addicted parents in health-care referents

National campaign to promote maternal and child health in 21st-century Japan Healthy Parents and Children 21

Service and Learning at a Residential Parenting Program for Incarcerated Mothers: Speech-Language Pathology Student Outcomes and Maternal Perspectives.

Progressive myelopathy in an adult

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The Parenting-Related Adverse Childhood Experiences Survey: A New Tool to Screen for Unhealthy Parenting in Pediatric Primary Care

Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report

Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report

A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next-generation sequencing and Sanger sequencing

Whole exome sequencing identifies a rare variant in DAAM2 as a potential candidate in idiopathic pulmonary ossification.

The clinical phenotype and genotype of NLRP12-autoinflammatory disease: a Chinese case series with literature review

Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder