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سندرم قاضی–مارکوئیزوس (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "سندرم قاضی–مارکوئیزوس" in Persian language version.

refsWebsite
Global rank Persian rank
3nih.gov
4th place
5th place
2doi.org
2nd place
2nd place
1web.archive.org
1st place
1st place
1omim.org
4,380th place
low place
1archive.org
6th place
9th place

archive.org

  • Qazi, QH; Markouizos, D; Rao, C; Sheikh, T; Beller, E; Kula, R (May 1994). "A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion". Journal of Medical Genetics. 31 (5): 405–9. doi:10.1136/jmg.31.5.405. PMC 1049875. PMID 8064821.

doi.org

  • Qazi, QH; Markouizos, D; Rao, C; Sheikh, T; Beller, E; Kula, R (May 1994). "A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion". Journal of Medical Genetics. 31 (5): 405–9. doi:10.1136/jmg.31.5.405. PMC 1049875. PMID 8064821.
  • Poznanski, AK; Garn, SM; Kuhns, LR; Sandusky, ST (November 1971). "Dysharmonic maturation of the hand in the congenital malformation syndromes". American Journal of Physical Anthropology. 35 (3): 417–32. doi:10.1002/ajpa.1330350322. PMID 4332712.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Qazi, QH; Markouizos, D; Rao, C; Sheikh, T; Beller, E; Kula, R (May 1994). "A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion". Journal of Medical Genetics. 31 (5): 405–9. doi:10.1136/jmg.31.5.405. PMC 1049875. PMID 8064821.
  • Poznanski, AK; Garn, SM; Kuhns, LR; Sandusky, ST (November 1971). "Dysharmonic maturation of the hand in the congenital malformation syndromes". American Journal of Physical Anthropology. 35 (3): 417–32. doi:10.1002/ajpa.1330350322. PMID 4332712.

ncbi.nlm.nih.gov

  • Qazi, QH; Markouizos, D; Rao, C; Sheikh, T; Beller, E; Kula, R (May 1994). "A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion". Journal of Medical Genetics. 31 (5): 405–9. doi:10.1136/jmg.31.5.405. PMC 1049875. PMID 8064821.

omim.org

  • «OMIM Entry - 600096 - PUERTO RICAN INFANT HYPOTONIA SYNDROME». بایگانی‌شده از اصلی در ۱۷ مه ۲۰۱۹. دریافت‌شده در ۳۰ دسامبر ۲۰۱۷.

web.archive.org

  • «OMIM Entry - 600096 - PUERTO RICAN INFANT HYPOTONIA SYNDROME». بایگانی‌شده از اصلی در ۱۷ مه ۲۰۱۹. دریافت‌شده در ۳۰ دسامبر ۲۰۱۷.