genetic Counselling

Adrenal hypoplasia congenita – an uncommon reason of primary adrenal insufficiency

Nuclear Receptor / Humans / Testosterone / genetic Counselling / Male / Androgens / Young Adult / Clinical Sciences / Adrenal Insufficiency / Late onset hypogonadism / Body Mass / Molecular Diagnosis / Nucleotides / Androgens / Young Adult / Clinical Sciences / Adrenal Insufficiency / Late onset hypogonadism / Body Mass / Molecular Diagnosis / Nucleotides

Maternal transmission in sporadic Huntington\'s disease

Neurology / Genetic counseling / Humans / genetic Counselling / Male / Polymerase Chain Reaction / Adult / Huntington disease / Family Study / Polymerase Chain Reaction / Adult / Huntington disease / Family Study

Maternal transmission in sporadic Huntington\'s disease

Neurology / Genetic counseling / Humans / genetic Counselling / Male / Polymerase Chain Reaction / Adult / Huntington disease / Family Study / Polymerase Chain Reaction / Adult / Huntington disease / Family Study

Tamizaje citogenético y molecular de la familia del gen DAZ en una población de hombres infértiles Cytogenetic and molecular screening of the DAZ gene family in a population of infertile males

Genetics / genetic Counselling / Population based study / Y chromosome / Gene Family

Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism

Genetics / Genetic counseling / Humans / genetic Counselling / Female / Siblings / Karyotyping / Gene Duplication / European / Fluorescent in situ hybridization / Mosaicism / Germ Cell / Growth Retardation / Siblings / Karyotyping / Gene Duplication / European / Fluorescent in situ hybridization / Mosaicism / Germ Cell / Growth Retardation

Diagnóstico molecular del retinoblastoma: epidemiología molecular y consejo genético

Molecular Epidemiology / Genetic counseling / Humans / Child / Mutation / genetic Counselling / Female / Male / Pedigree / Retinoblastoma / Medicina Clinica / retinoblastoma protein (RB1). / genetic Counselling / Female / Male / Pedigree / Retinoblastoma / Medicina Clinica / retinoblastoma protein (RB1).

Adrenal hypoplasia congenita – an uncommon reason of primary adrenal insufficiency

Nuclear Receptor / Humans / Testosterone / genetic Counselling / Male / Androgens / Young Adult / Clinical Sciences / Adrenal Insufficiency / Late onset hypogonadism / Body Mass / Molecular Diagnosis / Nucleotides / Androgens / Young Adult / Clinical Sciences / Adrenal Insufficiency / Late onset hypogonadism / Body Mass / Molecular Diagnosis / Nucleotides

PICOGEN: Five years experience with a genetic counselling program for dementia | PICOGEN: experiencia de 5 años de un programa de asesoramiento genético en demencia

Program Evaluation / Dementia / Genetic counseling / Humans / genetic Counselling / Genetic Screening / Neurologia / Aged / Middle Aged / Adult / Prion disease / Time Factors / Alzheimer Disease / Neurología / Genetic Screening / Neurologia / Aged / Middle Aged / Adult / Prion disease / Time Factors / Alzheimer Disease / Neurología

Guía diagnóstica en el paciente con enfermedad de Charcot-Marie-Tooth

Genetics / Molecular Epidemiology / Humans / Mutation / genetic Counselling / Neurologia / Conduction Velocity / CHarcot Marie Tooth / Autosomal Recessive / Molecular Diagnosis / Neurología / Charcot Marie Tooth Disease / Genetic Markers / Median Nerve / Neurologia / Conduction Velocity / CHarcot Marie Tooth / Autosomal Recessive / Molecular Diagnosis / Neurología / Charcot Marie Tooth Disease / Genetic Markers / Median Nerve

Diagnóstico molecular del retinoblastoma: epidemiología molecular y consejo genético

Molecular Epidemiology / genetic Counselling / Retinoblastoma / Medicina Clinica

Tamizaje citogenético y molecular de la familia del gen DAZ en una población de hombres infértiles

Genetics / genetic Counselling / Population based study / Y chromosome / Gene Family

Mutaciones de BRCA1 y BRCA2 en familias estudiadas en el Programa de Consejo Genético en el Cáncer de la Comunidad Valenciana

Breast Cancer / genetic Counselling / Medicina Clinica

Recomendaciones para el estudio genético de la pareja con alteraciones en la reproducción

Genetics / Family history / Medical History / Genetic Testing / genetic Counselling / Semen Analysis / Y chromosome / Laboratorio / DNA fragmentation / Semen Analysis / Y chromosome / Laboratorio / DNA fragmentation

Guía diagnóstica en el paciente con enfermedad de Charcot-Marie-Tooth

Genetics / Molecular Epidemiology / Humans / Mutation / genetic Counselling / Neurologia / Conduction Velocity / CHarcot Marie Tooth / Autosomal Recessive / Molecular Diagnosis / Neurología / Charcot Marie Tooth Disease / Genetic Markers / Median Nerve / Neurologia / Conduction Velocity / CHarcot Marie Tooth / Autosomal Recessive / Molecular Diagnosis / Neurología / Charcot Marie Tooth Disease / Genetic Markers / Median Nerve

Recomendaciones para el estudio genético de la pareja con alteraciones en la reproducción

Genetics / Family history / Medical History / Genetic Testing / genetic Counselling / Semen Analysis / Y chromosome / Laboratorio / DNA fragmentation / Semen Analysis / Y chromosome / Laboratorio / DNA fragmentation

Establishing a cancer genetics programme in Asia - the singapore experience

Genetics / Change Management / genetic Counselling / Indexation

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