Scalp defects-postaxial polydactyly syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Scalp defects-postaxial polydactyly syndrome" in English language version.

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doi.org

Fryns, J. P.; Van den Berghe, H. (1979-06-19). "Congenital scalp defects associated with postaxial polydactyly". Human Genetics. 49 (2): 217–219. doi:10.1007/BF00277645. ISSN 0340-6717. PMID 468253.
Buttiëns, M.; Fryns, J. P.; Jonckheere, P.; Brouckmans-Buttiëns, K.; Van den Berghe, H. (1985). "Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance". Human Genetics. 71 (1): 86–88. doi:10.1007/BF00295675. ISSN 0340-6717. PMID 4029956.

nih.gov

pubmed.ncbi.nlm.nih.gov

Fryns, J. P.; Van den Berghe, H. (1979-06-19). "Congenital scalp defects associated with postaxial polydactyly". Human Genetics. 49 (2): 217–219. doi:10.1007/BF00277645. ISSN 0340-6717. PMID 468253.
Buttiëns, M.; Fryns, J. P.; Jonckheere, P.; Brouckmans-Buttiëns, K.; Van den Berghe, H. (1985). "Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance". Human Genetics. 71 (1): 86–88. doi:10.1007/BF00295675. ISSN 0340-6717. PMID 4029956.

rarediseases.info.nih.gov

"Scalp defects postaxial polydactyly - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-06-11.

omim.org

"OMIM Entry - 181250 - SCALP DEFECTS AND POSTAXIAL POLYDACTYLY". omim.org. Retrieved 2022-06-11.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Scalp defects postaxial polydactyly syndrome". www.orpha.net. Retrieved 2022-06-11.{{cite web}}: CS1 maint: numeric names: authors list (link)

worldcat.org

search.worldcat.org

Fryns, J. P.; Van den Berghe, H. (1979-06-19). "Congenital scalp defects associated with postaxial polydactyly". Human Genetics. 49 (2): 217–219. doi:10.1007/BF00277645. ISSN 0340-6717. PMID 468253.
Buttiëns, M.; Fryns, J. P.; Jonckheere, P.; Brouckmans-Buttiëns, K.; Van den Berghe, H. (1985). "Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance". Human Genetics. 71 (1): 86–88. doi:10.1007/BF00295675. ISSN 0340-6717. PMID 4029956.