[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]

Assessment of physicians' resilience level during the COVID-19 pandemic.

Translational psychiatry·2021

Analysis of delays in the prescription of oseltamivir in hospitals and potential for improvement.

Medecine et maladies infectieuses·2018

[Impact of functional mass lesions in professional female singers : Biomechanics of vocal fold oscillation in the register transition regions].

HNO·2017

The effect of education plus access on perceived fruit and vegetable consumption in a rural African American community intervention.

Health education research·2015

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

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

[Autism, selective mutism and mild intellectual disability explained by 17q12 microdeletion syndrome].

Lakartidningen·2026

Automated Language Sample Analysis for Children With Developmental Language Disorder.

Journal of speech, language, and hearing research : JSLHR·2026

Sentence Completion Expressive Language Task-Preschool: Preliminary Evidence of Validity and Feasibility for the Neuroimaging Environment.

Journal of speech, language, and hearing research : JSLHR·2026

Correction: "Listening to the word autism changes everything": the impact of an Autism Spectrum disorder diagnosis on families.

Frontiers in psychology·2026

Toward early dyslexia screening through handwriting: A trustworthy XAI-enhanced deep learning framework.

Research in developmental disabilities·2026

Beyond Stuttering: Speech-Language Pathologists' Perceptions of Therapy for Children Who Stutter With Concomitant Speech and Language Needs.

Language, speech, and hearing services in schools·2026

Related Experiment Videos

[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]

Related Concept Videos

Assessment of physicians' resilience level during the COVID-19 pandemic.

Analysis of delays in the prescription of oseltamivir in hospitals and potential for improvement.

[Impact of functional mass lesions in professional female singers : Biomechanics of vocal fold oscillation in the register transition regions].

The effect of education plus access on perceived fruit and vegetable consumption in a rural African American community intervention.

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.

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.

[Autism, selective mutism and mild intellectual disability explained by 17q12 microdeletion syndrome].

Automated Language Sample Analysis for Children With Developmental Language Disorder.

Sentence Completion Expressive Language Task-Preschool: Preliminary Evidence of Validity and Feasibility for the Neuroimaging Environment.

Correction: "Listening to the word autism changes everything": the impact of an Autism Spectrum disorder diagnosis on families.

Toward early dyslexia screening through handwriting: A trustworthy XAI-enhanced deep learning framework.

Beyond Stuttering: Speech-Language Pathologists' Perceptions of Therapy for Children Who Stutter With Concomitant Speech and Language Needs.

Related Experiment Videos

[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]

Related Concept Videos

Related Articles