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Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred.
Am J Med Genet. 1990 Jul; 36(3):292-6.AJ

Abstract

A Pakistani kindred comprising 7 generations contained 7 men and 2 women with fibular hypoplasia and complex brachydactyly (syn: Du Pan syndrome). Analysis of the pedigree is strongly suggestive of autosomal recessive inheritance. The average inbreeding coefficient (F) for the affected persons was found to be significantly greater than that for unaffected persons in the pedigree and consanguineous loops could account for all affected persons being homozygous for the abnormal allele.

Authors+Show Affiliations

Department of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

2363425

Citation

Ahmad, M, et al. "Fibular Hypoplasia and Complex Brachydactyly (Du Pan Syndrome) in an Inbred Pakistani Kindred." American Journal of Medical Genetics, vol. 36, no. 3, 1990, pp. 292-6.
Ahmad M, Abbas H, Wahab A, et al. Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred. Am J Med Genet. 1990;36(3):292-6.
Ahmad, M., Abbas, H., Wahab, A., & Haque, S. (1990). Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred. American Journal of Medical Genetics, 36(3), 292-6.
Ahmad M, et al. Fibular Hypoplasia and Complex Brachydactyly (Du Pan Syndrome) in an Inbred Pakistani Kindred. Am J Med Genet. 1990;36(3):292-6. PubMed PMID: 2363425.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred. AU - Ahmad,M, AU - Abbas,H, AU - Wahab,A, AU - Haque,S, PY - 1990/7/1/pubmed PY - 1990/7/1/medline PY - 1990/7/1/entrez SP - 292 EP - 6 JF - American journal of medical genetics JO - Am J Med Genet VL - 36 IS - 3 N2 - A Pakistani kindred comprising 7 generations contained 7 men and 2 women with fibular hypoplasia and complex brachydactyly (syn: Du Pan syndrome). Analysis of the pedigree is strongly suggestive of autosomal recessive inheritance. The average inbreeding coefficient (F) for the affected persons was found to be significantly greater than that for unaffected persons in the pedigree and consanguineous loops could account for all affected persons being homozygous for the abnormal allele. SN - 0148-7299 UR - https://wwww.unboundmedicine.com/medline/citation/2363425/Fibular_hypoplasia_and_complex_brachydactyly__Du_Pan_syndrome__in_an_inbred_Pakistani_kindred_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1990&volume=36&issue=3&spage=292 DB - PRIME DP - Unbound Medicine ER -