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Postaxial acrofacial dysostosis (Miller) syndrome: a new case.
J Med Genet. 1991 Sep; 28(9):636-8.JM

Abstract

We describe a new case of postaxial acrofacial dysostosis (Miller) syndrome. This syndrome consists of mandibulofacial dysostosis, similar to that seen in Treacher Collins syndrome, and postaxial limb deficiency. The mode of inheritance remains uncertain.

Authors+Show Affiliations

Service de Médecine et Réanimation Néonatales, Maternité Régionale Universitaire, Nancy, France.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

1683410

Citation

Vigneron, J, et al. "Postaxial Acrofacial Dysostosis (Miller) Syndrome: a New Case." Journal of Medical Genetics, vol. 28, no. 9, 1991, pp. 636-8.
Vigneron J, Stricker M, Vert P, et al. Postaxial acrofacial dysostosis (Miller) syndrome: a new case. J Med Genet. 1991;28(9):636-8.
Vigneron, J., Stricker, M., Vert, P., Rousselot, J. M., & Levy, M. (1991). Postaxial acrofacial dysostosis (Miller) syndrome: a new case. Journal of Medical Genetics, 28(9), 636-8.
Vigneron J, et al. Postaxial Acrofacial Dysostosis (Miller) Syndrome: a New Case. J Med Genet. 1991;28(9):636-8. PubMed PMID: 1683410.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Postaxial acrofacial dysostosis (Miller) syndrome: a new case. AU - Vigneron,J, AU - Stricker,M, AU - Vert,P, AU - Rousselot,J M, AU - Levy,M, PY - 1991/9/1/pubmed PY - 1991/9/1/medline PY - 1991/9/1/entrez SP - 636 EP - 8 JF - Journal of medical genetics JO - J Med Genet VL - 28 IS - 9 N2 - We describe a new case of postaxial acrofacial dysostosis (Miller) syndrome. This syndrome consists of mandibulofacial dysostosis, similar to that seen in Treacher Collins syndrome, and postaxial limb deficiency. The mode of inheritance remains uncertain. SN - 0022-2593 UR - https://www.unboundmedicine.com/medline/citation/1683410/Postaxial_acrofacial_dysostosis__Miller__syndrome:_a_new_case_ L2 - https://jmg.bmj.com/lookup/pmidlookup?view=long&pmid=1683410 DB - PRIME DP - Unbound Medicine ER -