Two further males with female karyotypes

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Leukemia·2017

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

Leukemia·2016

MicroRNA-related sequence variations in human cancers.

Human genetics·2013

Recurrent and founder mutations in the PMS2 gene.

Clinical genetics·2012

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Clinical genetics·2011

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

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

Fertility Treatment Using Assisted Reproductive Technology During Immune Checkpoint Inhibition: Report of Two Cases.

The oncologist·2026

Reproductive healthcare use before and after infertility diagnosis: a population-based study in South Korea.

BMJ open·2026

Cost-effectiveness of safer conception strategies for HIV-discordant couples in Zimbabwe.

Journal of acquired immune deficiency syndromes (1999)·2026

Late-follicular androgen and estrogen rise associated with clinical pregnancy in IVF/ICSI with granulosa cell studies.

Reproduction & fertility·2026

Innovative treatment approaches for azoospermia: causes, emerging techniques, and future directions.

Molecular biology reports·2026

Effect of patient and partner preconceptional nutraceutical supplementation on the onset of natural pregnancy: a retrospective study.

Revista da Associacao Medica Brasileira (1992)·2026

Related Experiment Videos

Two further males with female karyotypes

Related Concept Videos

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

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.

Fertility Treatment Using Assisted Reproductive Technology During Immune Checkpoint Inhibition: Report of Two Cases.

Reproductive healthcare use before and after infertility diagnosis: a population-based study in South Korea.

Cost-effectiveness of safer conception strategies for HIV-discordant couples in Zimbabwe.

Late-follicular androgen and estrogen rise associated with clinical pregnancy in IVF/ICSI with granulosa cell studies.

Innovative treatment approaches for azoospermia: causes, emerging techniques, and future directions.

Effect of patient and partner preconceptional nutraceutical supplementation on the onset of natural pregnancy: a retrospective study.

Related Experiment Videos

Two further males with female karyotypes

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