Special Notice

Our website is undergoing changes and some listed testing may not be available any longer.  Except for Amish targeted testing and GAP testing, please call prior to ordering to be sure a test is available.

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DDC Clinic
Molecular Diagnostics Laboratory

Telephone: 440-632-5532
e-mail: lab@ddcclinic.org

Growth and Development (NGS Panels)

Growth and Development (NGS Panels)

List of available tests for this disease group.

ABCA12 Whole Gene Sequencing
ABCA12 Deletion and Duplication Analysis
Monogenic Diabetes Deletion and Duplication Panel
Monogenic Diabetes NGS Panel
Congenital Adrenal Hyperplasia Deletion and Duplication Panel
Congenital Adrenal Hyperplasia NGS Panel
Maturity-Onset Diabetes of the Young Deletion and Duplication Panel
Maturity-Onset Diabetes of the Young NGS Panel
Pseudohypoaldosteronism Type II Deletion and Duplication Panel
Pseudohypoaldosteronism Type II NGS Panel
Kallmann Syndrome Deletion and Duplication Panel
Kallmann Syndrome NGS Panel
Gitelman Syndrome Deletion and Duplication Panel
Gitelman Syndrome NGS Panel
Nephrogenic Diabetes Insipidus Deletion and Duplication Panel
Nephrogenic Diabetes Insipidus NGS Panel
Central Precocious Puberty Deletion and Duplication Panel
Central Precocious Puberty NGS Panel
Early Onset Obesity Deletion and Duplication Panel
Early Onset Obesity NGS Panel
Familial Hyperinsulinism Deletion and Duplication Panel
Familial Hyperinsulinism NGS Panel
Osteopetrosis, Autosomal Dominant Deletion and Duplication Panel
Osteopetrosis, Autosomal Dominant NGS Panel
Osteopetrosis Deletion and Duplication Panel
Osteopetrosis NGS Panel
Familial Hypercholanemia Deletion and Duplication Panel
Familial Hypercholanemia NGS Panel
Arthrogryposis Renal Dysfunction Cholestasis Deletion and Duplication Panel
Arthrogryposis Renal Dysfunction Cholestasis NGS Panel
Alagille Syndrome Deletion and Duplication Panel
Alagille Syndrome NGS Panel
Jaundice Deletion and Duplication Panel
Jaundice NGS Panel
Bile Acid Synthesis Defect Deletion and Duplication Panel
Bile Acid Synthesis Defect NGS Panel
Progressive Familial Intrahepatic Cholestasis Deletion and Duplication Panel
Progressive Familial Intrahepatic Cholestasis NGS Panel
Short Stature, Autosomal Recessive Deletion and Duplication Panel
Short Stature, Autosomal Recessive NGS Panel
Seckel Syndrome Deletion and Duplication Panel
Seckel Syndrome NGS Panel
Combined Pituitary Hormone Deficiency Deletion and Duplication Panel
Combined Pituitary Hormone Deficiency NGS Panel
Overgrowth and Intellectual Disability Deletion and Duplication Panel
Overgrowth and Intellectual Disability NGS Panel
Noonan Syndrome and Related Disorders Deletion and Duplication Panel
Noonan Syndrome and Related Disorders NGS Panel
Noonan Syndrome Deletion and Duplication Panel
Noonan Syndrome NGS Panel
Neurofibromatosis Deletion and Duplication Panel
Neurofibromatosis NGS Panel
Tuberous Sclerosis Complex Deletion and Duplication Panel
Tuberous Sclerosis Complex NGS Panel
Microcephalic Osteodysplastic Primordial Dwarfism Deletion and Duplication Panel
Microcephalic Osteodysplastic Primordial Dwarfism NGS Panel
Meier-Gorlin Syndrome Deletion and Duplication Panel
Meier-Gorlin Syndrome NGS Panel
Marfan Syndrome Deletion and Duplication Panel
Marfan Syndrome NGS Panel
Isolated Growth Hormone Deficiency Deletion and Duplication Panel
Isolated Growth Hormone Deficiency NGS Panel
Cowden Syndrome Deletion and Duplication Panel
Cowden Syndrome NGS Panel
Cornelia de Lange Deletion and Duplication Analysis Panel
Cornelia de Lange NGS Panel
Congenital Hypothyroidism, Nongoitrous Deletion and Duplication Panel
Congenital Hypothyroidism, Nongoitrous NGS Panel
Congenital Cataract Deletion and Duplication Panel
Congenital Cataract NGS Panel
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