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.
MeSH
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 -