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Institut de Pathologie et de Genetique, Centre de Genetique Humaine

Disorder	Genes	Test Method	Lab Info	Product code
Antenatal Bartter Syndrome Type 1 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Antenatal Bartter Syndrome Type 1	SLC12A1,	Sequence analysis of the entire coding region		CODE: 17111	Add to Cart Add to Compare List
Antenatal Bartter Syndrome Type 2 - Sequence analysis of select exons	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Antenatal Bartter Syndrome Type 2	KCNJ1,	Sequence analysis of select exons		CODE: 17113	Add to Cart Add to Compare List
Antenatal Bartter Syndrome Type 2 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Antenatal Bartter Syndrome Type 2	KCNJ1,	Sequence analysis of the entire coding region		CODE: 17112	Add to Cart Add to Compare List
Ataxia with Oculomotor Apraxia 1 - Deletion/duplication analysis	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Ataxia with Oculomotor Apraxia 1	APTX,	Deletion/duplication analysis		CODE: 17115	Add to Cart Add to Compare List
Ataxia with Oculomotor Apraxia 1 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Ataxia with Oculomotor Apraxia 1	APTX,	Sequence analysis of the entire coding region		CODE: 17114	Add to Cart Add to Compare List
Bartter Syndrome Type 3 - Deletion/duplication analysis	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Bartter Syndrome Type 3	CLCNKB,	Deletion/duplication analysis		CODE: 17117	Add to Cart Add to Compare List
Bartter Syndrome Type 3 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Bartter Syndrome Type 3	CLCNKB,	Sequence analysis of the entire coding region		CODE: 17116	Add to Cart Add to Compare List
Berardinelli-Seip Congenital Lipodystrophy Type 1 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Berardinelli-Seip Congenital Lipodystrophy Type 1		Sequence analysis of the entire coding region		CODE: 17118	Add to Cart Add to Compare List
Berardinelli-Seip Congenital Lipodystrophy Type 2 - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Berardinelli-Seip Congenital Lipodystrophy Type 2		Sequence analysis of the entire coding region		CODE: 17119	Add to Cart Add to Compare List
BSCL2-Related Neurologic Disorders/Seipinopathy - Sequence analysis of select exons	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	BSCL2-Related Neurologic Disorders/Seipinopathy	BSCL2,	Sequence analysis of select exons		CODE: 17120	Add to Cart Add to Compare List
Calpainopathy - Deletion/duplication analysis	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Calpainopathy		Deletion/duplication analysis		CODE: 17122	Add to Cart Add to Compare List
Calpainopathy - Sequence analysis of the entire coding region	Institut de Pathologie et de Genetique, Centre de Genetique Humaine	Calpainopathy		Sequence analysis of the entire coding region		CODE: 17121	Add to Cart Add to Compare List

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