Zane's Diagnostic Odyssey: His Mother's Story in Honor of Undiagnosed Day - National Organization for Rare Disorders
What Does MMIHS Look Like? – MMIHS
MMIHS Foundation (@MMIHSFoundation) / X
The MMIHS Foundation, Inc. | Nonprofit organization
MJHS FOUNDATION - GuideStar Profile
The MMIHS Foundation, Inc. | Nonprofit organization
Team MMIHS Merchandise Custom Ink Fundraising
BU Research Blog | Erasmus+ exchange visit to Nepal by Dr. Rebecca Neal | Bournemouth University
Fundraiser by Sarah Turman : Ava's $10 for 10th birthday fundraiser for MMIHS
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome | PLOS Genetics
Manmohan Memorial Institute of Health Sciences - The Edu Fair Nepal
LMOD1 - The Genomic Medicine FoundationThe Genomic Medicine Foundation | Current Trends in Genomic Medicine & Cardiovascular Genetics and Genomics
The MMIHS Foundation, Inc. | Nonprofit organization
MMIHS – Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
Team MMIHS Merchandise Custom Ink Fundraising
NORD and the Galactosemia Foundation Jointly Publish First “Voice of the Patient” Report to Help Inform the FDA and Researchers - National Organization for Rare Disorders
The MMIHS Foundation, Inc. | Nonprofit organization
David Foster Foundation Summer 2021 Newsletter by David Foster Foundation - Issuu
National Organization for Rare Disorders Announces More Than $100,000 in Grant Funding Available for Rare Disease Research
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation – MMIHS
Ava Gets Support For Her Rare GI Condition - Children's Health
The MMIHS Foundation, Inc. | Nonprofit organization
Unexpected discovery offers rare disease hope - SVI
