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Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III.
Am J Med Genet 1985; 21(3):569-74AJ

Abstract

We describe a female infant with low birthweight osteodysplastic microcephalic dwarfism. The child has many manifestations in common with those seen in osteodysplastic primordial dwarfism types I and III. The classification of this heterogeneous group of disorders is discussed in the light of the above case.

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

4025388

Citation

Winter, R M., et al. "Osteodysplastic Primordial Dwarfism: Report of a Further Patient With Manifestations Similar to Those Seen in Patients With Types I and III." American Journal of Medical Genetics, vol. 21, no. 3, 1985, pp. 569-74.
Winter RM, Wigglesworth J, Harding BN. Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III. Am J Med Genet. 1985;21(3):569-74.
Winter, R. M., Wigglesworth, J., & Harding, B. N. (1985). Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III. American Journal of Medical Genetics, 21(3), pp. 569-74.
Winter RM, Wigglesworth J, Harding BN. Osteodysplastic Primordial Dwarfism: Report of a Further Patient With Manifestations Similar to Those Seen in Patients With Types I and III. Am J Med Genet. 1985;21(3):569-74. PubMed PMID: 4025388.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III. AU - Winter,R M, AU - Wigglesworth,J, AU - Harding,B N, PY - 1985/7/1/pubmed PY - 1985/7/1/medline PY - 1985/7/1/entrez SP - 569 EP - 74 JF - American journal of medical genetics JO - Am. J. Med. Genet. VL - 21 IS - 3 N2 - We describe a female infant with low birthweight osteodysplastic microcephalic dwarfism. The child has many manifestations in common with those seen in osteodysplastic primordial dwarfism types I and III. The classification of this heterogeneous group of disorders is discussed in the light of the above case. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/4025388/Osteodysplastic_primordial_dwarfism:_report_of_a_further_patient_with_manifestations_similar_to_those_seen_in_patients_with_types_I_and_III_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1985&volume=21&issue=3&spage=569 DB - PRIME DP - Unbound Medicine ER -