whole-exome sequencing – Soft Bones

Compound Heterozygous PIGT Mutations in Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome: First Case in Korea and Characterization by Persistent Hypophosphatasia

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Denise Goodbar June 30, 2021

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Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia

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Denise Goodbar May 18, 2021

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141 Hawkins Place, #267
Boonton, NJ 07005, USA.

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