[Blood chimerism in dizygotic twins]

[Differentiated thyroid gland carcinomas in "autonomous adenomas" in childhood].

Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen·1995

Parturition in the rabbit is compromised by daytime nursing: the role of oxytocin.

Biology of reproduction·1995

Detection of microsporidia (Enterocytozoon bieneusi) in intestinal biopsy specimens from human immunodeficiency virus-infected patients by PCR.

Journal of clinical microbiology·1995

Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine.

Cellular signalling·1995

Immediate metabolic effects of different nutritional regimens in critically ill medical patients.

Intensive care medicine·1995

[Residual placental blood and bone marrow as sources of hematopoietic stem cells for allogenic stem cell transplantation. Comparative analysis of hematopoietic potential].

Klinische Padiatrie·1995

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

American journal of medical genetics. Part A·2026

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

Nature genetics·2026

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Cureus·2026

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Molecular syndromology·2026

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

Journal of immunology (Baltimore, Md. : 1950)·2026

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Arquivos de neuro-psiquiatria·2026

Related Experiment Videos

[Blood chimerism in dizygotic twins]

Related Concept Videos

[Differentiated thyroid gland carcinomas in "autonomous adenomas" in childhood].

Parturition in the rabbit is compromised by daytime nursing: the role of oxytocin.

Detection of microsporidia (Enterocytozoon bieneusi) in intestinal biopsy specimens from human immunodeficiency virus-infected patients by PCR.

Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine.

Immediate metabolic effects of different nutritional regimens in critically ill medical patients.

[Residual placental blood and bone marrow as sources of hematopoietic stem cells for allogenic stem cell transplantation. Comparative analysis of hematopoietic potential].

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Related Experiment Videos

[Blood chimerism in dizygotic twins]

Related Concept Videos

Related Articles