Search Results - Siriwan, Pichit

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    A Novel Mutation in EFNB1, Probably with a Dominant Negative Effect, Underlying Craniofrontonasal Syndrome

    A Novel Mutation in EFNB1, Probably with a Dominant Negative Effect, Underlying Craniofrontonasal Syndrome by Shotelersuk, Vorasuk, Siriwan, Pichit, Ausavarat, Surasawadee

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Are there any changes in burden and management of communicable diseases in areas affected by Cyclone Nargis?

    Are there any changes in burden and management of communicable diseases in areas affected by Cyclone Nargis? by Myint, Nyan Win, Kaewkungwal, Jaranit, Singhasivanon, Pratap, Chaisiri, Kamron, Panjapiyakul, Pornpet, Siriwan, Pichit, Mallik, Arun K, Nyein, Soe Lwin, Mu, Thet Thet

    Published in Conflict and health
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    PDGFRa mutations in humans with isolated cleft palate

    PDGFRa mutations in humans with isolated cleft palate by RATTANASOPHA, Sawitree, TONGKOBPETCH, Siraprapa, SRICHOMTHONG, Chalurmpon, SIRIWAN, Pichit, SUPHAPEETIPORN, Kanya, SHOTELERSUK, Vorasuk

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects

    Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects by Leoyklang, Petcharat, Suphapeetiporn, Kanya, Siriwan, Pichit, Desudchit, Tayard, Chaowanapanja, Pattraporn, Gahl, William A, Shotelersuk, Vorasuk

    Published in Human mutation
    Get full text
    Article
    Save to List
    Saved in:
  5. 5
    Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome

    Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome by Yeetong, Patra, Mahatumarat, Charan, Siriwan, Pichit, Rojvachiranonda, Nond, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele

    Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele by Suphapeetiporn, Kanya, Mahatumarat, Charan, Rojvachiranonda, Nond, Taecholarn, Chopiew, Siriwan, Pichit, Srivuthana, Sumarlee, Shotelersuk, Vorasuk

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    Heterozygous nonsense mutationSATB2 associated with cleft palate, osteoporosis, and cognitive defects

    Heterozygous nonsense mutationSATB2 associated with cleft palate, osteoporosis, and cognitive defects by Leoyklang, Petcharat, Suphapeetiporn, Kanya, Siriwan, Pichit, Desudchit, Tayard, Chaowanapanja, Pattraporn, Gahl, William A, Shotelersuk, Vorasuk

    Published in Human mutation
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    A Novel Mutation in EFNB1, Probably With a Dominant-Negative Effect, Underlying Craniofrontonasal Syndrome

    A Novel Mutation in EFNB1, Probably With a Dominant-Negative Effect, Underlying Craniofrontonasal Syndrome by Shotelersuk, Vorasuk, Siriwan, Pichit, Ausavarat, Surasawadee

    Get full text
    Article
    Save to List
    Saved in:
  9. 9
    Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome

    Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome by Yeetong, Patra, Mahatumarat, Charan, Siriwan, Pichit, Rojvachiranonda, Nond, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk

    Get full text
    Report
    Save to List
    Saved in:

Search Tools: