Familial reinclusion of permanent molars

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome.

BMC medical genetics·2015

Monitoring of risk factor/outcome combinations: a valuable supplement to birth defect monitoring.

The International journal of risk & safety in medicine·2013

Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency.

Journal of inherited metabolic disease·2008

[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].

Nederlands tijdschrift voor geneeskunde·2006

Preconceptional screening of couples for carriers of cystic fibrosis: a prospective evaluation of effects, costs and savings for different mutation detection methods.

Community genetics·2004

Explorative study of costs, effects and savings of screening for female fragile X premutation and full mutation carriers in the general population.

Community genetics·2004

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Correction: Comparative Analysis of Image Quality Assessment Between Digital Single-Lens Reflex (DSLR) Camera and Smartphone Camera for Dental Photography.

Cureus·2026

Phosphomimetic statherin-derived peptide protects against intrinsic enamel erosion independently of sodium trimetaphosphate.

European journal of oral sciences·2026

Influence of Illumination Conditions and Cross-Polarization on DSLR-Based Clinical Tooth Color Assessment: A Comparison With Spectrophotometric Measurements.

Journal of esthetic and restorative dentistry : official publication of the American Academy of Esthetic Dentistry ... [et al.]·2026

Early orthopedic treatment of skeletal Class III malocclusion: Correlating dentoskeletal changes with psychosocial outcomes using the modified SEC III protocol and PIDAQ.

Journal of the World federation of orthodontists·2026

Detection of the presence of second mesiobuccal canal in the maxillary first molar with bitewing radiography using MediXpar.

Morphologie : bulletin de l'Association des anatomistes·2026

PLXDC2-OT-peptide Promotes the Odontogenic/Osteogenic Differentiation of SCAPs via the PI3K-AKT Signalling Pathway.

International dental journal·2026

Related Experiment Videos

Familial reinclusion of permanent molars

Related Concept Videos

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome.

Monitoring of risk factor/outcome combinations: a valuable supplement to birth defect monitoring.

Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency.

[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].

Preconceptional screening of couples for carriers of cystic fibrosis: a prospective evaluation of effects, costs and savings for different mutation detection methods.

Explorative study of costs, effects and savings of screening for female fragile X premutation and full mutation carriers in the general population.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Correction: Comparative Analysis of Image Quality Assessment Between Digital Single-Lens Reflex (DSLR) Camera and Smartphone Camera for Dental Photography.

Phosphomimetic statherin-derived peptide protects against intrinsic enamel erosion independently of sodium trimetaphosphate.

Influence of Illumination Conditions and Cross-Polarization on DSLR-Based Clinical Tooth Color Assessment: A Comparison With Spectrophotometric Measurements.

Early orthopedic treatment of skeletal Class III malocclusion: Correlating dentoskeletal changes with psychosocial outcomes using the modified SEC III protocol and PIDAQ.

Detection of the presence of second mesiobuccal canal in the maxillary first molar with bitewing radiography using MediXpar.

PLXDC2-OT-peptide Promotes the Odontogenic/Osteogenic Differentiation of SCAPs via the PI3K-AKT Signalling Pathway.

Related Experiment Videos

Familial reinclusion of permanent molars

Abstract:

Related Concept Videos

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