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Results 11 - 20 of 9,281 for 3S -"3-Hydroxyadipyl-CoA"
  1. Developmental milestones record - 3 years 
    ... skills and growth markers that are relevant to 3-year-olds. ... provider. Physical and motor milestones for a typical 3-year-old include: Gains about 4 to 5 ...
    https://medlineplus.gov/ency/article/002014.htm - Medical Encyclopedia
  2. Acetaminophen and Codeine 
    Empracet® (#3, #4) ... Papa-deine® (#3, #4) ... Phenaphen® with Codeine (#2, #3, #4) ... Proval® #3 ... Tylenol® with Codeine (#3, #4) ... Additional doses may be given every 2 to 3 minutes, if symptoms return before medical help arrives. ...
    https://medlineplus.gov/druginfo/meds/a601005.html - Drugs and Supplements
  3. 3-M syndrome 
    3-M syndrome is a disorder that causes skeletal abnormalities including short stature (dwarfism) and unusual facial features. The name of this condition ...
    https://medlineplus.gov/genetics/condition/3-m-syndrome - Genetics
  4. 5q31.3 microdeletion syndrome 
    5q31.3 microdeletion syndrome is a condition characterized by severely delayed development of speech and motor skills, such as ... difficulty swallowing (dysphagia) can be life-threatening.5q31.3 microdeletion syndrome is also characterized by distinctive facial ...
    https://medlineplus.gov/.../condition/5q313-microdeletion-syndrome - Genetics
  5. 22q13.3 deletion syndrome 
    22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome, is a disorder caused by the loss ... of the chromosome at a location designated q13.3.The features of 22q13.3 deletion syndrome vary ...
    https://medlineplus.gov/genetics/condition/22q133-deletion-syndrome - Genetics
  6. Atelosteogenesis type 3 
    Atelosteogenesis type 3 is a disorder that affects the development of bones throughout the body. Affected individuals are born with inward- ... mouth (a cleft palate.)Individuals with atelosteogenesis type 3 typically have an underdeveloped rib cage that affects ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-3 - Genetics
  7. Spinocerebellar ataxia type 3 
    Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  8. 17-beta hydroxysteroid dehydrogenase 3 deficiency 
    17-beta hydroxysteroid dehydrogenase 3 deficiency is a condition that affects male sexual development. People with this condition are genetically male, ...
    https://medlineplus.gov/...hydroxysteroid-dehydrogenase-3-deficiency - Genetics
  9. Preschooler development 
    ... normal social and physical development of children ages 3 to 6 years old includes many developmental milestones. ... child's health care provider. PHYSICAL DEVELOPMENT The typical 3- to 6-year-old: Gains about 4 to ...
    https://medlineplus.gov/ency/article/002013.htm - Medical Encyclopedia
  10. Miconazole Vaginal 
    Monistat® 3 Combination Pack® ... Monistat® 3 Suppositories ... 1) or once a day at bedtime for 3 days in a row (Monistat 3). The vaginal cream is used once a day ...
    https://medlineplus.gov/druginfo/meds/a601203.html - Drugs and Supplements
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