Down syndrome: correspondence of clinical diagnosis and karyotype

The value of beta trace protein in CSF-leakage detection confirmed by endoscopic fluorescein evaluation.

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Gender-specific differences in feasibility of pre-lacrimal window approach.

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Prenatal cigarette smoke exposure slightly alters neurobehavioral development in neonatal rats: Implications for developmental origins of health and disease (DoHAD).

Physiology international·2020

Disturbed spermatogenic signaling in pituitary adenylate cyclase activating polypeptide-deficient mice.

Reproduction (Cambridge, England)·2017

Pituitary Adenylate Cyclase Activating Polypeptide, A Potential Therapeutic Agent for Diabetic Retinopathy in Rats: Focus on the Vertical Information Processing Pathway.

Neurotoxicity research·2016

Ischemia/reperfusion-induced Kidney Injury in Heterozygous PACAP-deficient Mice.

Transplantation proceedings·2015

Intrauterine weight retardation and the concomitant length retardation: a statistical analysis of anthropometric data.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

Hormonal control of sodium content in human milk.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

The prognosis of severe bronchial asthma in childhood on the basis of late reexaminations.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

HLA antigens in bullous epidermolysis, congenital ichthyosis and ectodermal dysplasia.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

Congenital postural deformity association.

Acta paediatrica Academiae Scientiarum Hungaricae·1982

Female-specific alterations in insulin dynamics are associated with glucose tolerance in a Glut1DS mouse model.

Disease models & mechanisms·2026

The uneven landscape of cognitive domains in 22q11.2 deletion syndrome: A large consortium study.

Psychological medicine·2026

Circulating Family with Sequence Similarity 19, Member A5 as a Potential Indicator of Atherogenic Risk: Correlations with Low-Density Lipoprotein/Apolipoprotein B Ratio, Atherogenic Index, and Castelli Indices in Diet-Induced Obesity.

Iranian journal of medical sciences·2026

Biliverdin reductase A deficiency reveals sex- and brain region-specific vulnerability to high-fat diet feeding.

Redox biology·2026

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Mutation research. Reviews in mutation research·2026

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

AJP reports·2026

Related Experiment Videos

Down syndrome: correspondence of clinical diagnosis and karyotype

Related Concept Videos

The value of beta trace protein in CSF-leakage detection confirmed by endoscopic fluorescein evaluation.

Gender-specific differences in feasibility of pre-lacrimal window approach.

Prenatal cigarette smoke exposure slightly alters neurobehavioral development in neonatal rats: Implications for developmental origins of health and disease (DoHAD).

Disturbed spermatogenic signaling in pituitary adenylate cyclase activating polypeptide-deficient mice.

Pituitary Adenylate Cyclase Activating Polypeptide, A Potential Therapeutic Agent for Diabetic Retinopathy in Rats: Focus on the Vertical Information Processing Pathway.

Ischemia/reperfusion-induced Kidney Injury in Heterozygous PACAP-deficient Mice.

Intrauterine weight retardation and the concomitant length retardation: a statistical analysis of anthropometric data.

Hormonal control of sodium content in human milk.

Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation.

The prognosis of severe bronchial asthma in childhood on the basis of late reexaminations.

HLA antigens in bullous epidermolysis, congenital ichthyosis and ectodermal dysplasia.

Congenital postural deformity association.

Female-specific alterations in insulin dynamics are associated with glucose tolerance in a Glut1DS mouse model.

The uneven landscape of cognitive domains in 22q11.2 deletion syndrome: A large consortium study.

Circulating Family with Sequence Similarity 19, Member A5 as a Potential Indicator of Atherogenic Risk: Correlations with Low-Density Lipoprotein/Apolipoprotein B Ratio, Atherogenic Index, and Castelli Indices in Diet-Induced Obesity.

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Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

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Down syndrome: correspondence of clinical diagnosis and karyotype

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