Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 145 for dms
  1. Epidermolysis bullosa simplex 
    Epidermolysis bullosa simplex is one of a group of genetic conditions called epidermolysis bullosa that cause the skin to be very fragile and to blister easily. Blisters ...
    https://medlineplus.gov/.../condition/epidermolysis-bullosa-simplex - Genetics
  2. 22q11.2 deletion syndrome 
    ... 09297040590911185. Citation on PubMed Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, ... M, Pinto-Martin J, Zackai EH, McDonald-McGinn DM, Emanuel BS. Autism spectrum disorders and symptoms in ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  3. Glutaric acidemia type I 
    ... I; GA1 PubMed Basinger AA, Booker JK, Frazier DM, Koeberl DD, Sullivan JA, Muenzer J. Glutaric acidemia ... CR, Harting I, Hoffmann GF, Karall D, Koeller DM, Krawinkel MB, Okun JG, Opladen T, Posset R, ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  4. Familial thoracic aortic aneurysm and dissection 
    ... A, LeMaire SA, Franco LM, Coselli JS, Milewicz DM, Belmont JW. FBN1 mutations in patients with descending ... Grand Opportunity Exome Sequencing Project; Kim C, Milewicz DM. Recurrent gain-of-function mutation in PRKG1 causes ...
    https://medlineplus.gov/...l-thoracic-aortic-aneurysm-and-dissection - Genetics
  5. Robinow syndrome 
    ... T, Brunner HG, Lai A, Kunst HP, Markie DM, Robertson SP. Mutations in DVL1 cause an osteosclerotic ... E, Vulto-van Silfhout AT, Steehouwer M, Muzny DM, Sutton VR, Gibbs RA; Baylor-Hopkins Center for ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  6. CHARGE syndrome 
    ... Central Hale CL, Niederriter AN, Green GE, Martin DM. Atypical phenotypes associated with pathogenic CHD7 variants and ... Ravenswaaij-Arts CM, Hefner M, Blake K, Martin DM. CHD7 Disorder. 2006 Oct 2 [updated 2022 Sep ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  7. Hereditary neuralgic amyotrophy 
    ... EK, Miller LR, Betz B, Buchan JG, Knutzen DM, Barnett K, Landsverk ML, Brice A, LeGuern E, ... JM, Windebank AJ, Dyck PJ, Friedenberg SM, Klein DM, Dyck PJ. SEPT9 mutations and a conserved 17q25 ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  8. Immune thrombocytopenia 
    ... 64(12):1358-62. Citation on PubMed Arnold DM. Bleeding complications in immune thrombocytopenia. Hematology Am Soc ... GR, Goy J, Nazi I, Kelton JG, Arnold DM. Severe bleeding events in adults and children with ...
    https://medlineplus.gov/genetics/condition/immune-thrombocytopenia - Genetics
  9. Chordoma 
    ... J, Burdette L, Yeager M, Chanock SJ, Parry DM, Goldstein AM, Yang XR. Characterization of T gene ... Epub 2010 Nov 24. Citation on PubMed Sciubba DM, Chi JH, Rhines LD, Gokaslan ZL. Chordoma of ...
    https://medlineplus.gov/genetics/condition/chordoma - Genetics
  10. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... Taylor RW, Abdel-All Z, Lightowlers RN, Turnbull DM. Molecular neuropathology of MELAS: level of heteroplasmy in ... 2(1):30-4. Citation on PubMed Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next