Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Leukemia·2010

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Leukemia·2010

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Journal of medical genetics·2006

Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.

Annales de genetique·2001

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.

Chromosoma·2001

Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.

Genetics in medicine : official journal of the American College of Medical Genetics·2001

Defects of blastogenesis.

American journal of medical genetics·2002

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

American journal of medical genetics·2002

Limb anomalies: Developmental and evolutionary aspects.

American journal of medical genetics·2002

Molecular etiology of gut malformations and diseases.

American journal of medical genetics·2002

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

American journal of medical genetics·2002

Three cases of tetrasomy 9p.

American journal of medical genetics·2002

Cardiometabolic Risk Factors, Obesity Phenotypes, and Novel Anthropometric Indices in Patients With Acute Coronary Syndrome: A Hospital-Based Case-Control Study in Central India.

Cureus·2026

Bedside Flexible Bronchoscopy in the Neonatal Intensive Care Unit: Current Evidence, Clinical Applications and Future Directions.

Respiratory medicine·2026

Decreased function of fatty acid desaturase 1 is associated with placental foetal vascular malperfusion and highlights the key role of the maternal-foetal interface.

EBioMedicine·2026

MRI-based correlation of cry acoustic parameters and brain structural development in preterm infants.

Acta psychologica·2026

Determinants of low birth weight among newborns in selected public hospitals in Southwest Ethiopia: a multi-center unmatched case-control study.

Sexual & reproductive healthcare : official journal of the Swedish Association of Midwives·2026

Haplotype structure and functional genotype-phenotype interactions of PON1 (L55M/Q192R) variants in Egyptian children with nephrotic syndrome.

Molecular biology reports·2026

Related Experiment Videos

Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant

Related Concept Videos

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.

Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.

Defects of blastogenesis.

Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.

Limb anomalies: Developmental and evolutionary aspects.

Molecular etiology of gut malformations and diseases.

Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).

Three cases of tetrasomy 9p.

Cardiometabolic Risk Factors, Obesity Phenotypes, and Novel Anthropometric Indices in Patients With Acute Coronary Syndrome: A Hospital-Based Case-Control Study in Central India.

Bedside Flexible Bronchoscopy in the Neonatal Intensive Care Unit: Current Evidence, Clinical Applications and Future Directions.

Decreased function of fatty acid desaturase 1 is associated with placental foetal vascular malperfusion and highlights the key role of the maternal-foetal interface.

MRI-based correlation of cry acoustic parameters and brain structural development in preterm infants.

Determinants of low birth weight among newborns in selected public hospitals in Southwest Ethiopia: a multi-center unmatched case-control study.

Haplotype structure and functional genotype-phenotype interactions of PON1 (L55M/Q192R) variants in Egyptian children with nephrotic syndrome.

Related Experiment Videos

Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant

Abstract:

Related Concept Videos

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