MMIHS – Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
Ava Gets Support For Her Rare GI Condition - Children's Health
The MMIHS Foundation, Inc. | Nonprofit organization
MMIHS DAY! – Attitude & Intestinal Fortitude
Unexpected discovery offers rare disease hope - SVI
Team MMIHS Merchandise Custom Ink Fundraising
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation, Inc. | Nonprofit organization
MMIHS – Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
The MMIHS Foundation, Inc. | Nonprofit organization
LMOD1 - The Genomic Medicine FoundationThe Genomic Medicine Foundation | Current Trends in Genomic Medicine & Cardiovascular Genetics and Genomics
The MMIHS Foundation, Inc. | Nonprofit organization
Fundraiser by Sarah Turman : Ava's $10 for 10th birthday fundraiser for MMIHS
Team MMIHS Merchandise Custom Ink Fundraising
What Does MMIHS Look Like? – MMIHS
Zane's Diagnostic Odyssey: His Mother's Story in Honor of Undiagnosed Day - National Organization for Rare Disorders
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation, Inc. | Nonprofit organization
NORD Announces over $100,000 in Grant Funding Available for Rare Disease Research
What Does MMIHS Look Like? – MMIHS
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome | PLOS Genetics
