[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]

Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders.

Molecular human reproduction·2021

Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.

European journal of medical genetics·2019

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.

European journal of medical genetics·2018

MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype.

Neurogenetics·2018

[Changes in clinical practice related to the arrival of next-generation sequencing in the genetic diagnosis of developmental diseases].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2018

[Renal abnormalities in Down syndrome: A review].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2017

[Neuroprotection for preterm infants with antenatal magnesium sulphate].

Journal de gynecologie, obstetrique et biologie de la reproduction·2017

[Is universal screening for cervical length among singleton pregnancies with no history of preterm birth justified?]

Journal de gynecologie, obstetrique et biologie de la reproduction·2017

[Lifestyle recommendations for prevention of spontaneous preterm birth in asymptomatic pregnant women].

Journal de gynecologie, obstetrique et biologie de la reproduction·2017

[Psychological aspects of abortion].

Journal de gynecologie, obstetrique et biologie de la reproduction·2016

[Tocolysis for preterm labor without premature preterm rupture of membranes].

Journal de gynecologie, obstetrique et biologie de la reproduction·2016

[Prediction of preterm delivery in symptomatic women (preterm labor)].

Journal de gynecologie, obstetrique et biologie de la reproduction·2016

Whole-genome sequencing identifies a potentially causative homozygous splicing variant in RAD54 like in non-obstructive azoospermia.

International journal of reproductive biomedicine·2026

FAN1 mutation and karyomegalic nephropathy in chronic kidney disease.

BMJ case reports·2026

The Quasi-Systematic Nature of Splitter Cells.

Neural computation·2026

Chromosome Editing Using the Lambda Red Recombinase System in Chlamydia trachomatis and Chlamydia muridarum.

Methods in molecular biology (Clifton, N.J.)·2026

Decoding cell division history and lineage-resolved phenotypic patterns from single-cell barcode and transcriptomic data.

Genome research·2026

Spatial genome organization in nematodes with programmed DNA elimination.

Genome research·2026

Related Experiment Videos

[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]

Related Concept Videos

Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders.

Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.

MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype.

[Changes in clinical practice related to the arrival of next-generation sequencing in the genetic diagnosis of developmental diseases].

[Renal abnormalities in Down syndrome: A review].

[Neuroprotection for preterm infants with antenatal magnesium sulphate].

[Is universal screening for cervical length among singleton pregnancies with no history of preterm birth justified?]

[Lifestyle recommendations for prevention of spontaneous preterm birth in asymptomatic pregnant women].

[Psychological aspects of abortion].

[Tocolysis for preterm labor without premature preterm rupture of membranes].

[Prediction of preterm delivery in symptomatic women (preterm labor)].

Whole-genome sequencing identifies a potentially causative homozygous splicing variant in RAD54 like in non-obstructive azoospermia.

FAN1 mutation and karyomegalic nephropathy in chronic kidney disease.

The Quasi-Systematic Nature of Splitter Cells.

Chromosome Editing Using the Lambda Red Recombinase System in Chlamydia trachomatis and Chlamydia muridarum.

Decoding cell division history and lineage-resolved phenotypic patterns from single-cell barcode and transcriptomic data.

Spatial genome organization in nematodes with programmed DNA elimination.

Related Experiment Videos

[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities]

Related Concept Videos

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