[Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility]

Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.

Clinical genetics·2015

Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid.

European journal of medical genetics·2013

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH.

Clinical genetics·2012

[Microsurgical tubal desterilization: an efficient procedure. Evaluation of a 42 cases cohort according to Guzick's biparametric method].

Gynecologie, obstetrique & fertilite·2009

19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.

Journal of medical genetics·2009

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.

Human reproduction (Oxford, England)·2007

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

Characterisation of the Novel HLA-DQA1*04:01:11 Allele by Next-Generation Sequencing.

HLA·2026

Characterisation of the Novel HLA-DQB1*03:612 Allele by Sequencing-Based Typing.

HLA·2026

Identification of a New HLA-DRB5 Allele in a Chinese Han Individual, HLA-DRB5*01:01:17.

HLA·2026

The Novel HLA-DPB1*1903:01 Allele Was Likely Generated by a Recombination Event.

HLA·2026

Characterisation of the Novel HLA-C*16:01:53 Allele by Next-Generation Sequencing.

HLA·2026

Identification of the Novel HLA-F*01:37 Allele Using PolyseqOne Sequencing.

HLA·2026

Related Experiment Videos

[Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility]

Related Concept Videos

Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.

Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid.

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH.

[Microsurgical tubal desterilization: an efficient procedure. Evaluation of a 42 cases cohort according to Guzick's biparametric method].

19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.

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.

Characterisation of the Novel HLA-DQA1*04:01:11 Allele by Next-Generation Sequencing.

Characterisation of the Novel HLA-DQB1*03:612 Allele by Sequencing-Based Typing.

Identification of a New HLA-DRB5 Allele in a Chinese Han Individual, HLA-DRB5*01:01:17.

The Novel HLA-DPB1*1903:01 Allele Was Likely Generated by a Recombination Event.

Characterisation of the Novel HLA-C*16:01:53 Allele by Next-Generation Sequencing.

Identification of the Novel HLA-F*01:37 Allele Using PolyseqOne Sequencing.

Related Experiment Videos

[Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility]

Abstract:

Related Concept Videos

Related Articles