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The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family.
Eur J Pediatr. 1981 May; 136(2):217-20.EJ

Abstract

A severe expression of the Greig polysyndactyly-craniofacial dysmorphism syndrome is reported in two dizygotic 4-month-old twin brothers. A minor expression of this autosomal dominant syndrome was present in the father.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

6262085

Citation

Fryns, J P., et al. "The Greig Polysyndactyly Craniofacial Dysmorphism Syndrome: Variable Expression in a Family." European Journal of Pediatrics, vol. 136, no. 2, 1981, pp. 217-20.
Fryns JP, Van Noyen G, Van den Berghe H. The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family. Eur J Pediatr. 1981;136(2):217-20.
Fryns, J. P., Van Noyen, G., & Van den Berghe, H. (1981). The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family. European Journal of Pediatrics, 136(2), 217-20.
Fryns JP, Van Noyen G, Van den Berghe H. The Greig Polysyndactyly Craniofacial Dysmorphism Syndrome: Variable Expression in a Family. Eur J Pediatr. 1981;136(2):217-20. PubMed PMID: 6262085.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family. AU - Fryns,J P, AU - Van Noyen,G, AU - Van den Berghe,H, PY - 1981/5/1/pubmed PY - 1981/5/1/medline PY - 1981/5/1/entrez SP - 217 EP - 20 JF - European journal of pediatrics JO - Eur J Pediatr VL - 136 IS - 2 N2 - A severe expression of the Greig polysyndactyly-craniofacial dysmorphism syndrome is reported in two dizygotic 4-month-old twin brothers. A minor expression of this autosomal dominant syndrome was present in the father. SN - 0340-6199 UR - https://www.unboundmedicine.com/medline/citation/6262085/The_Greig_polysyndactyly_craniofacial_dysmorphism_syndrome:_variable_expression_in_a_family_ L2 - http://www.diseaseinfosearch.org/result/5854 DB - PRIME DP - Unbound Medicine ER -