[Ring chromosome 18. 18p-/18q- -deletion-syndrome]

Long bones after suspected "grave robbery": a comparison of different methods for the estimation of the post mortem interval.

Forensic science, medicine, and pathology·2025

Search for Lepton Number and Flavor Violation in K^{+} and π^{0} Decays.

Physical review letters·2021

No Difference in the Phenotypic Expression of Frailty among Elderly Patients Recently Diagnosed with Cancer Vs Cancer Free Patients.

The journal of nutrition, health & aging·2020

Isotensor Dibaryon in the pp→ppπ^{+}π^{-} Reaction?

Physical review letters·2018

Spin Dependence of η Meson Production in Proton-Proton Collisions Close to Threshold.

Physical review letters·2018

[Practical implementation of an integrated care model in mother-child treatment].

Der Nervenarzt·2016

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

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

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

Gene·2026

Developmental Profiles Associated with TUBA1A, TUBB2A, TUBB2B, and TUBB3 Tubulinopathy Conditions.

American journal on intellectual and developmental disabilities·2026

Related Experiment Videos

[Ring chromosome 18. 18p-/18q- -deletion-syndrome]

Related Concept Videos

Long bones after suspected "grave robbery": a comparison of different methods for the estimation of the post mortem interval.

Search for Lepton Number and Flavor Violation in K^{+} and π^{0} Decays.

No Difference in the Phenotypic Expression of Frailty among Elderly Patients Recently Diagnosed with Cancer Vs Cancer Free Patients.

Isotensor Dibaryon in the pp→ppπ^{+}π^{-} Reaction?

Spin Dependence of η Meson Production in Proton-Proton Collisions Close to Threshold.

[Practical implementation of an integrated care model in mother-child treatment].

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

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.

Expanding the clinical and molecular spectrum of SETD5, NEDD4L, and TBL1X related disorders: A case report and literature review.

Developmental Profiles Associated with TUBA1A, TUBB2A, TUBB2B, and TUBB3 Tubulinopathy Conditions.

Related Experiment Videos

[Ring chromosome 18. 18p-/18q- -deletion-syndrome]

Related Concept Videos

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