[Craniofacial development: morphogenesis and determinism]

Same author

Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2021

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Heterogeneity in defining fetal corpus callosal pathology: systematic review.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2020

Same author

Re-focusing on Agnathia-Otocephaly complex.

Clinical oral investigations·2020

Same author

Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2019

Same author

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2017

Same author

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia.

Clinical genetics·2016

Same journal

Point-of-care capillary blood ketone testing to predict the need for intravenous or nasogastric tube rehydration in children with acute gastroenteritis.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Same journal

Transition practices of patients with inflammatory bowel disease from pediatric to adult healthcare systems. Results from a national survey.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Related Experiment Videos

[Craniofacial development: morphogenesis and determinism]

Related Concept Videos

Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment.

Heterogeneity in defining fetal corpus callosal pathology: systematic review.

Re-focusing on Agnathia-Otocephaly complex.

Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis.

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia.

Family experiences of paediatric palliative care during hospital-at-home: a systematic review.

Knowledge of maternity caregivers on vaccination BCG recommendations and circuits.

"CRANIOQUALITY study: Quality of life in children with non-syndromic craniosynostosis after surgery".

Chronological evolution of brain imaging of hemiconvulsion-hemiplegia-epilepsy from 5 cases in Mayotte island.

Point-of-care capillary blood ketone testing to predict the need for intravenous or nasogastric tube rehydration in children with acute gastroenteritis.

Transition practices of patients with inflammatory bowel disease from pediatric to adult healthcare systems. Results from a national survey.

Related Experiment Videos

[Craniofacial development: morphogenesis and determinism]

Related Concept Videos

Related Articles

Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment.

Heterogeneity in defining fetal corpus callosal pathology: systematic review.

Re-focusing on Agnathia-Otocephaly complex.

Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis.

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia.

Family experiences of paediatric palliative care during hospital-at-home: a systematic review.

Knowledge of maternity caregivers on vaccination BCG recommendations and circuits.

"CRANIOQUALITY study: Quality of life in children with non-syndromic craniosynostosis after surgery".

Chronological evolution of brain imaging of hemiconvulsion-hemiplegia-epilepsy from 5 cases in Mayotte island.

Point-of-care capillary blood ketone testing to predict the need for intravenous or nasogastric tube rehydration in children with acute gastroenteritis.

Transition practices of patients with inflammatory bowel disease from pediatric to adult healthcare systems. Results from a national survey.