Intrauterine diagnosis and management of genetic defects

Analysis of human spermatozoa for Y chromosomal nondisjunction.

Teratogenesis, carcinogenesis, and mutagenesis·1980

A survey of X chromatin in the newborn.

Biology of the neonate·1976

Use of methenamine hippurate in male infertility.

Urology·1975

Fabry's disease: antenatal detection.

Science (New York, N.Y.)·1971

Autosomal trisomy in a chimpanzee: resemblance to Down's syndrome.

Science (New York, N.Y.)·1969

Management of Multiple Sclerosis During Pregnancy and the Reproductive Years in 2026: An Expert Clinical Review.

American journal of obstetrics and gynecology·2026

Incidence, survival, and symptoms at recurrence among vulvar cancer patients treated with curative intent: a population-based cohort study.

American journal of obstetrics and gynecology·2026

Clinical Trajectories and MRI-Based Triage of Uterine Leiomyoma Molecular Subtypes: A Large-Scale Retrospective Analysis of 720 Genotyped Tumors.

American journal of obstetrics and gynecology·2026

Neonatal outcomes in gestational diabetes trials: What clinicians should consider when interpreting treatment effects.

American journal of obstetrics and gynecology·2026

Intra-amniotic Categories of Preterm Prelabor Rupture of Membranes: Gestational Age-Specific Distribution, Amniotic fluid Microbial Profiles, and Neonatal Outcomes.

American journal of obstetrics and gynecology·2026

From polycystic ovary syndrome to polyendocrine metabolic ovarian syndrome: what obstetricians and gynecologists need to know.

American journal of obstetrics and gynecology·2026

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

Appreciating diversity: a review of the Iranian genomic landscape.

European journal of human genetics : EJHG·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Related Experiment Videos

Intrauterine diagnosis and management of genetic defects

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Analysis of human spermatozoa for Y chromosomal nondisjunction.

A survey of X chromatin in the newborn.

Use of methenamine hippurate in male infertility.

Fabry's disease: antenatal detection.

Autosomal trisomy in a chimpanzee: resemblance to Down's syndrome.

Management of Multiple Sclerosis During Pregnancy and the Reproductive Years in 2026: An Expert Clinical Review.

Incidence, survival, and symptoms at recurrence among vulvar cancer patients treated with curative intent: a population-based cohort study.

Clinical Trajectories and MRI-Based Triage of Uterine Leiomyoma Molecular Subtypes: A Large-Scale Retrospective Analysis of 720 Genotyped Tumors.

Neonatal outcomes in gestational diabetes trials: What clinicians should consider when interpreting treatment effects.

Intra-amniotic Categories of Preterm Prelabor Rupture of Membranes: Gestational Age-Specific Distribution, Amniotic fluid Microbial Profiles, and Neonatal Outcomes.

From polycystic ovary syndrome to polyendocrine metabolic ovarian syndrome: what obstetricians and gynecologists need to know.

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Appreciating diversity: a review of the Iranian genomic landscape.

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

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Intrauterine diagnosis and management of genetic defects

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