[Strategies for the delivery of genetic counseling in Chile]

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.

Cell death and differentiation·2016

Provisionally unique autosomal recessive syndrome due to significant consanguinity.

American journal of medical genetics·2001

Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome.

Journal of child neurology·2000

Ring 2 chromosome: ten-year follow-up report.

American journal of medical genetics·1999

Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?

American journal of medical genetics·1999

Radiological and orthopedic abnormalities in Satoyoshi syndrome.

Pediatric radiology·1997

Percepciones y creencias sobre criopreservación embrionaria en mujeres y hombres que se realizan técnicas de reproducción asistida en Santiago, Chile.

Revista chilena de obstetricia y ginecologia·2020

[Regulation of uterine blood flow. II. Functions of estrogen and estrogen receptor α/β in genomic and non-genomic actions of the uterine endothelium].

Revista chilena de obstetricia y ginecologia·2015

[Regulation of uterine blood flow. I. Functions of estrogen and estrogen receptor α/β in the uterine vascular endothelium during pregnancy].

Revista chilena de obstetricia y ginecologia·2015

[Exceptional variety of endometrial cancer].

Revista chilena de obstetricia y ginecologia·1995

[Pregnancy and the use of pacemakers].

Revista chilena de obstetricia y ginecologia·1995

[Cystic hamartoma: prenatal diagnosis and follow-up of newborn infants].

Revista chilena de obstetricia y ginecologia·1995

Comparative genome assemblies reveal distinct allelic and structural variation at blast resistance loci in rice CT21375-F4-4 and Moroberekan.

The plant genome·2026

Introgression under linear selection on continuous genomes.

Genetics·2026

Screening for beta thalassemia trait in a heterogeneous university-based population in Delhi-NCR, India.

Journal of community genetics·2026

Genome-wide characterisation of leaf rust resistance loci in an Eastern European barley collection.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.

Human mutation·2026

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs.

Frontiers in genetics·2026

Related Experiment Videos

[Strategies for the delivery of genetic counseling in Chile]

Related Concept Videos

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.

Provisionally unique autosomal recessive syndrome due to significant consanguinity.

Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome.

Ring 2 chromosome: ten-year follow-up report.

Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?

Radiological and orthopedic abnormalities in Satoyoshi syndrome.

Percepciones y creencias sobre criopreservación embrionaria en mujeres y hombres que se realizan técnicas de reproducción asistida en Santiago, Chile.

[Regulation of uterine blood flow. II. Functions of estrogen and estrogen receptor α/β in genomic and non-genomic actions of the uterine endothelium].

[Regulation of uterine blood flow. I. Functions of estrogen and estrogen receptor α/β in the uterine vascular endothelium during pregnancy].

[Exceptional variety of endometrial cancer].

[Pregnancy and the use of pacemakers].

[Cystic hamartoma: prenatal diagnosis and follow-up of newborn infants].

Comparative genome assemblies reveal distinct allelic and structural variation at blast resistance loci in rice CT21375-F4-4 and Moroberekan.

Introgression under linear selection on continuous genomes.

Screening for beta thalassemia trait in a heterogeneous university-based population in Delhi-NCR, India.

Genome-wide characterisation of leaf rust resistance loci in an Eastern European barley collection.

Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs.

Related Experiment Videos

[Strategies for the delivery of genetic counseling in Chile]

Related Concept Videos

Related Articles