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All Children's Hospital, Clinical Molecular Genetics Laboratory

Disorder	Genes	Test Method	Lab Info	Product code
Achondroplasia - Sequence analysis of select exons	All Children's Hospital, Clinical Molecular Genetics Laboratory	Achondroplasia	FGFR3,	Sequence analysis of select exons		CODE: 1842	Add to Cart Add to Compare List
Hypochondroplasia - Sequence analysis of select exons	All Children's Hospital, Clinical Molecular Genetics Laboratory	Hypochondroplasia	FGFR3,	Sequence analysis of select exons		CODE: 1863	Add to Cart Add to Compare List
17-beta Hydroxysteroid Dehydrogenase III Deficiency - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	17-beta Hydroxysteroid Dehydrogenase III Deficiency	HSD17B3,	Sequence analysis of the entire coding region		CODE: 1841	Add to Cart Add to Compare List
ACTH Deficiency - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	ACTH Deficiency	TBX19,	Sequence analysis of the entire coding region		CODE: 1843	Add to Cart Add to Compare List
Angelman Syndrome - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	Angelman Syndrome	UBE3A,	Sequence analysis of the entire coding region		CODE: 1845	Add to Cart Add to Compare List
Angelman Syndrome - Methylation analysis	All Children's Hospital, Clinical Molecular Genetics Laboratory	Angelman Syndrome	UBE3A,	Methylation analysis		CODE: 1846	Add to Cart Add to Compare List
Angelman Syndrome - Uniparental disomy study (UPD)	All Children's Hospital, Clinical Molecular Genetics Laboratory	Angelman Syndrome	UBE3A,	Uniparental disomy study (UPD)		CODE: 1847	Add to Cart Add to Compare List
Aromatase Deficiency - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	Aromatase Deficiency	CYP19A1,	Sequence analysis of the entire coding region		CODE: 1848	Add to Cart Add to Compare List
Athyroidal Hypothyroidism with Spiky Hair and Cleft Palate - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	Athyroidal Hypothyroidism with Spiky Hair and Cleft Palate	FOXE1,	Sequence analysis of the entire coding region		CODE: 1849	Add to Cart Add to Compare List
Axenfeld-Rieger Syndrome, Type 1 - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	Axenfeld-Rieger Syndrome, Type 1	PITX2,	Sequence analysis of the entire coding region		CODE: 1850	Add to Cart Add to Compare List
Chromosome 7-Related Russell-Silver Syndrome - Uniparental disomy study (UPD)	All Children's Hospital, Clinical Molecular Genetics Laboratory	Chromosome 7-Related Russell-Silver Syndrome		Uniparental disomy study (UPD)		CODE: 1851	Add to Cart Add to Compare List
PTEN Hamartoma Tumor Syndrome (PHTS) - Sequence analysis of the entire coding region	All Children's Hospital, Clinical Molecular Genetics Laboratory	PTEN Hamartoma Tumor Syndrome (PHTS)	PTEN,	Sequence analysis of the entire coding region		CODE: 1887	Add to Cart Add to Compare List

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