Синдром Пфайффера (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Синдром Пфайффера" in Ukrainian language version.

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2,888^th place

1,066^th place

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doi.org (Global: 2^nd place; Ukrainian: 4^th place)

Vogels A., Fryns J.P. Pfeiffer syndrome // Orphanet Journal of Rare Diseases^[en]. — 2006. — Vol. 1 (18 January). — P. 19. — DOI:10.1186/1750-1172-1-19. — PMID 16740155 .
Chan C.T., Thorogood P. Pleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial development // Pediatric Research^[en] : journal. — 1999. — Vol. 45, no. 1 (1). — P. 46—53. — DOI:10.1203/00006450-199901000-00008. — PMID 9890607 .

Pfeiffer R.A. Dominant Hereditary Acrocephalosyndactylia // European Journal of Pediatrics^[en]. — 1964. — Т. 90 (18 січня). — С. 301—320. — PMID 14316612 .
Vogels A., Fryns J.P. Pfeiffer syndrome // Orphanet Journal of Rare Diseases^[en]. — 2006. — Vol. 1 (18 January). — P. 19. — DOI:10.1186/1750-1172-1-19. — PMID 16740155 .
Chan C.T., Thorogood P. Pleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial development // Pediatric Research^[en] : journal. — 1999. — Vol. 45, no. 1 (1). — P. 46—53. — DOI:10.1203/00006450-199901000-00008. — PMID 9890607 .

Pfeiffer R.A. Dominant Hereditary Acrocephalosyndactylia // European Journal of Pediatrics^[en]. — 1964. — Т. 90 (18 січня). — С. 301—320. — PMID 14316612 .
Vogels A., Fryns J.P. Pfeiffer syndrome // Orphanet Journal of Rare Diseases^[en]. — 2006. — Vol. 1 (18 January). — P. 19. — DOI:10.1186/1750-1172-1-19. — PMID 16740155 .
Chan C.T., Thorogood P. Pleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial development // Pediatric Research^[en] : journal. — 1999. — Vol. 45, no. 1 (1). — P. 46—53. — DOI:10.1203/00006450-199901000-00008. — PMID 9890607 .