Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2

A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.

Human mutation·2001

Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.

The Journal of clinical endocrinology and metabolism·2001

Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1.

American journal of human genetics·2001

Genetics of craniofacial development and malformation.

Nature reviews. Genetics·2001

Craniosynostosis and related limb anomalies.

Novartis Foundation symposium·2001

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.

Nature genetics·2001

Bone mineral density in the growing human mandible.

Journal of craniofacial genetics and developmental biology·2001

Palate vault morphology in Down syndrome.

Journal of craniofacial genetics and developmental biology·2001

Interrelation between fusions in the primary dentition and agenesis in the succedaneous permanent dentition seen from an embryological point of view.

Journal of craniofacial genetics and developmental biology·2001

Correlation of HSP110 expression with all-trans retinoic acid-induced apoptosis.

Journal of craniofacial genetics and developmental biology·2001

Secalonic acid D alters the expression and phosphorylation of the transcription factors and their binding to cAMP response element in developing murine secondary palate.

Journal of craniofacial genetics and developmental biology·2001

Dentition development and budding morphogenesis.

Journal of craniofacial genetics and developmental biology·2001

State-Funded Health Insurance Expansion for Noncitizen Immigrants and Hospital Uncompensated Care.

JAMA network open·2026

Erratum: The Revista Panamericana de Salud Pública/Pan American Journal of Public Health draws readers' attention to an unintentional error in the following article.

Revista panamericana de salud publica = Pan American journal of public health·2026

The many faces of RAG deficiency.

Haematologica·2026

Hematoma, Hemarthrosis, and Hemotympanum: A Case Report of Acquired Hemophilia A.

Journal of education & teaching in emergency medicine·2026

Are There Differences in Return-to-Work Experiences for Workers Who Acquired COVID-19 at Work Compared to Workers who Sustained a Non-COVID-19 Work-Related Injury or Illness?

Journal of occupational rehabilitation·2026

Related Experiment Videos

Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2

Related Concept Videos

A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.

Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.

Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1.

Genetics of craniofacial development and malformation.

Craniosynostosis and related limb anomalies.

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.

Bone mineral density in the growing human mandible.

Palate vault morphology in Down syndrome.

Interrelation between fusions in the primary dentition and agenesis in the succedaneous permanent dentition seen from an embryological point of view.

Correlation of HSP110 expression with all-trans retinoic acid-induced apoptosis.

Secalonic acid D alters the expression and phosphorylation of the transcription factors and their binding to cAMP response element in developing murine secondary palate.

Dentition development and budding morphogenesis.

State-Funded Health Insurance Expansion for Noncitizen Immigrants and Hospital Uncompensated Care.

Erratum: The Revista Panamericana de Salud Pública/Pan American Journal of Public Health draws readers' attention to an unintentional error in the following article.

The many faces of RAG deficiency.

Hematoma, Hemarthrosis, and Hemotympanum: A Case Report of Acquired Hemophilia A.

Are There Differences in Return-to-Work Experiences for Workers Who Acquired COVID-19 at Work Compared to Workers who Sustained a Non-COVID-19 Work-Related Injury or Illness?

Related Experiment Videos

Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2

Related Concept Videos

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