[Screening for fetal chromosomal anomalies--recent aspects]

[Analysis of prenatal follow-up strategies for trisomy 21 affected pregnancies in France].

Gynecologie, obstetrique, fertilite & senologie·2017

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Molecular psychiatry·2015

Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.

Clinical genetics·2013

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.

Journal of medical genetics·2009

A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein.

Human genetics·2008

Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q).

Prenatal diagnosis·2005

[Lucy's cancer(s): A prehistorical origin?]

Gynecologie, obstetrique & fertilite·2016

[Male age in assisted reproductive technologies: Is there a limit?]

Gynecologie, obstetrique & fertilite·2016

[Iodinated contrast in pregnant women and neonatal thyroid function].

Gynecologie, obstetrique & fertilite·2016

[Breast cancer and diabetes mellitus: Complex interactions].

Gynecologie, obstetrique & fertilite·2016

[Why and how to perform an ultrasound-guided transversus abdominis plane block: A step-by-step approach].

Gynecologie, obstetrique & fertilite·2016

[Does post operative sonographic position of preventive cervical cerclage affect gestational age at birth?]

Gynecologie, obstetrique & fertilite·2016

Divergent C. elegans toxin alleles are suppressed by distinct mechanisms.

eLife·2026

"Male Predominance and Pubertal Resolution in Vernal Keratoconjunctivitis: Exploring Associations with Ocular Surface Sex Steroid Intracrinology".

The ocular surface·2026

Social isolation upregulates takeout expression in female Drosophila melanogaster to promote sucrose preference.

PLoS genetics·2026

Interplay of βPS and βν integrins in Drosophila muscle functioning.

Gene·2026

Unilateral Thyroid Hypoplasia With Isthmic Absence and Presence of Pyramidal Lobe and Levator Glandulae Thyroidae: A Cadaveric Case Report.

Cureus·2026

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Acta crystallographica. Section F, Structural biology communications·2026

Related Experiment Videos

[Screening for fetal chromosomal anomalies--recent aspects]

Related Concept Videos

[Analysis of prenatal follow-up strategies for trisomy 21 affected pregnancies in France].

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.

A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein.

Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q).

[Lucy's cancer(s): A prehistorical origin?]

[Male age in assisted reproductive technologies: Is there a limit?]

[Iodinated contrast in pregnant women and neonatal thyroid function].

[Breast cancer and diabetes mellitus: Complex interactions].

[Why and how to perform an ultrasound-guided transversus abdominis plane block: A step-by-step approach].

[Does post operative sonographic position of preventive cervical cerclage affect gestational age at birth?]

Divergent C. elegans toxin alleles are suppressed by distinct mechanisms.

"Male Predominance and Pubertal Resolution in Vernal Keratoconjunctivitis: Exploring Associations with Ocular Surface Sex Steroid Intracrinology".

Social isolation upregulates takeout expression in female Drosophila melanogaster to promote sucrose preference.

Interplay of βPS and βν integrins in Drosophila muscle functioning.

Unilateral Thyroid Hypoplasia With Isthmic Absence and Presence of Pyramidal Lobe and Levator Glandulae Thyroidae: A Cadaveric Case Report.

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Related Experiment Videos

[Screening for fetal chromosomal anomalies--recent aspects]

Related Concept Videos

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