Monozygosity and holoprosencephaly: cleavage disorders of the "midline field"

A support group for couples who have terminated a pregnancy after prenatal diagnosis: Recurrent themes and observations.

Journal of genetic counseling·2013

Survey of pediatrician practices in retrieving statewide authorized newborn screening results.

Pediatrics·2001

Interstitial insertion of Y-specific DNA sequences including SRY into chromosome 4 in a 45,X male child.

American journal of medical genetics·1997

Congenital diaphragmatic hernia and ipsilateral limb reduction defect: a new case, long-term follow-up and review of the literature.

Clinical dysmorphology·1997

Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.

American journal of medical genetics·1997

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.

Prenatal diagnosis·1996

Defects of blastogenesis.

American journal of medical genetics·2002

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

American journal of medical genetics·2002

Limb anomalies: Developmental and evolutionary aspects.

American journal of medical genetics·2002

Molecular etiology of gut malformations and diseases.

American journal of medical genetics·2002

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

American journal of medical genetics·2002

Three cases of tetrasomy 9p.

American journal of medical genetics·2002

Curating the Fetal Genome: Experience of the ClinGen Prenatal Gene Curation Expert Panel (GCEP).

Prenatal diagnosis·2026

Combating of hippocampal neuroinflammatory response by folic acid: helpful prospective in autistic-like phenotype induced following maternal separation stress.

The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry·2026

APOE-centered transcriptional convergence underlying diverse dementia subtypes.

Journal of Alzheimer's disease : JAD·2026

Novel Transvalvular Flow Criteria Reduce Indeterminate Stress Echocardiography and Refine Risk Stratification in Low-Gradient Aortic Stenosis.

Circulation. Cardiovascular imaging·2026

A rare de novo contiguous 15q11.1-q13.3 duplication with tetrasomy (CN=4) and adjacent trisomy (CN=3) associated with severe global developmental delay, autism spectrum disorder, and subclinical epileptiform discharges: a case report and literature review.

Frontiers in genetics·2026

TRIM28 contributes to epidermal homeostasis and is associated with altered p53 regulation.

Frontiers in cell and developmental biology·2026

Related Experiment Videos

Monozygosity and holoprosencephaly: cleavage disorders of the "midline field"

Related Concept Videos

A support group for couples who have terminated a pregnancy after prenatal diagnosis: Recurrent themes and observations.

Survey of pediatrician practices in retrieving statewide authorized newborn screening results.

Interstitial insertion of Y-specific DNA sequences including SRY into chromosome 4 in a 45,X male child.

Congenital diaphragmatic hernia and ipsilateral limb reduction defect: a new case, long-term follow-up and review of the literature.

Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.

Defects of blastogenesis.

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

Limb anomalies: Developmental and evolutionary aspects.

Molecular etiology of gut malformations and diseases.

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Three cases of tetrasomy 9p.

Curating the Fetal Genome: Experience of the ClinGen Prenatal Gene Curation Expert Panel (GCEP).

Combating of hippocampal neuroinflammatory response by folic acid: helpful prospective in autistic-like phenotype induced following maternal separation stress.

APOE-centered transcriptional convergence underlying diverse dementia subtypes.

Novel Transvalvular Flow Criteria Reduce Indeterminate Stress Echocardiography and Refine Risk Stratification in Low-Gradient Aortic Stenosis.

A rare de novo contiguous 15q11.1-q13.3 duplication with tetrasomy (CN=4) and adjacent trisomy (CN=3) associated with severe global developmental delay, autism spectrum disorder, and subclinical epileptiform discharges: a case report and literature review.

TRIM28 contributes to epidermal homeostasis and is associated with altered p53 regulation.

Related Experiment Videos

Monozygosity and holoprosencephaly: cleavage disorders of the "midline field"

Related Concept Videos

Related Articles