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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Miraca Genetics Laboratories
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Educational Materials

Amniocentesis
Amniocentesis
Biochemical Testing
Biochemical Testing
Biochemical Testing
BluePrint Panel
Cancer Cytogenetics
Cancer Cytogenetics
Cancer Chromosomal Microarray Analysis (CMA) Guide
Cancer Chromosomal Microarray Analysis (CMA) Guide
Cancer Exome Sequencing
Cancer Exome Sequencing
CGL Information
Cancer Information & Testing
Hereditary Cancer Panels V2
Hereditary Cancer Panels V.3
Hereditary Breast Cancer Panels Patient Guide
Hereditary Breast Cancer Panels Patient Guide
Cancer Gene Mutation Panel V.2 Flyer
Cancer Gene Mutation Panel V.2 Flyer
Leukemia Mutation Panel
Leukemia Mutation Panel
Chorionic Villus Sampling
Chorionic Villus Sampling (CVS)
Chromosomal Microarray Analysis (CMA)
Chromosomal Microarray Analysis (CMA)
Chromosomal Microarray Analysis Options
Chromosomal Microarray Analysis (CMA) - Information on CMA-HR, CMA-SNP, and CMA-Comprehensive
Counseling Aid for Chromosomal Microarray Analysis
Counseling Aid for Chromosomal Microarray Analysis (CMA)
Cystic Fibrosis Testing
Cystic Fibrosis Testing
GeneAware Reproductive Carrier Screen Disease Information
GeneAware Reproductive Carrier Screen Disease Information
GeneAware Reproductive Carrier Screen Information for Patients
GeneAware Reproductive Carrier Screen Information for Patients
GeneAware Reproductive Carrier Screen Information for Providers
GeneAware Reproductive Carrier Screen Information for Providers
Genetic Counseling
Genetic Counseling
Genetic Testing for Patients with Autism
Genetic Testing for Autism Spectrum Disorders
Genetic Testing for Patients with Autism
Global MAPS (Metabolomic Assisted Pathway Screen)
Comprehensive Diagnosis for Mitochondrial Disorders
Comprehensive Diagnosis for Mitochondrial Disorders
Mitochondrial AlgorithmRecommended Clinical Testing Algorithm for Mitochondrial Disorder
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
BCM MitomeNGS-SM Eye Panels
Comprehensive Molecular Diagnosis for Human Genetic Disorders
Non-Invasive Prenatal Screening Patient Guide
Patient Guide for Non-Invasive Prenatal Screening Options
Non-Invasive Prenatal Deletion Test
Non-Invasive Prenatal Deletion Test Information

Prenatal Testing
Prenatal Testing

Prenatal Chromosomal Microarray Analysis Expanded and Targeted Arrays
Prenatal Chromosomal Microarray Analysis: Expanded and Targeted Arrays

Prenatal Chromosomal Microarray Analysis
Prenatal Chromosomal Microarray Analysis

Prenatal Chromosomal Microarray Analysis Brochure - English
Prenatal Chromosomal Microarray Analysis Brochure - English

Prenatal Chromosomal Microarray Analysis Brochure - Spanish
Prenatal Chromosomal Microarray Analysis Brochure - Spanish

Prenatal Chromosomal Microarray Analysis FAQs
Prenatal Chromosomal Microarray Analysis FAQs

Recommended Flowchart for Lowe Syndrome Diagnostic Testing
Recommended Flowchart for Lowe Syndrome Diagnostic Testing

Whole Exome Sequencing
Whole Exome Sequencing

Whole Exome Sequencing Information for Patients and Families FlyerWhole Exome Sequencing (WES): Information for Patients and Families (Flyer)

Whole Exome Sequencing Information for Patients and Families Brochure
Whole Exome Sequencing (WES): Information for Patients and Families (Brochure)

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