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Guadalajara camptodactyly syndrome type II.
Clin Genet. 1985 Jul; 28(1):54-60.CG

Abstract

Two sisters and an unrelated girl presented a distinct intrauterine growth retardation-malformation syndrome with short stature, microcephaly, pectus excavatum, hip dislocation, hypoplastic pubic region and genitalia, camptodactyly, talipes, shortened 2nd toes, hypoplastic patella and skeletal dysplasia probably due to homozygosity from an autosomal recessive gene.

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Publisher Full Text

Authors

Cantú JM
No affiliation info available
García-Cruz D
No affiliation info available
Gil-Viera J
No affiliation info available
Nazará Z
No affiliation info available
Ramírez ML
No affiliation info available
Solé-Pujol MT
No affiliation info available
Sánchez-Corona J
No affiliation info available

MeSH

Abnormalities, MultipleChild, PreschoolDermatoglyphicsFemaleFetal Growth RetardationFingersHumansPregnancySyndrome

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

4040823

Citation

Cantú, J M., et al. "Guadalajara Camptodactyly Syndrome Type II." Clinical Genetics, vol. 28, no. 1, 1985, pp. 54-60.
Cantú JM, García-Cruz D, Gil-Viera J, et al. Guadalajara camptodactyly syndrome type II. Clin Genet. 1985;28(1):54-60.
Cantú, J. M., García-Cruz, D., Gil-Viera, J., Nazará, Z., Ramírez, M. L., Solé-Pujol, M. T., & Sánchez-Corona, J. (1985). Guadalajara camptodactyly syndrome type II. Clinical Genetics, 28(1), 54-60.
Cantú JM, et al. Guadalajara Camptodactyly Syndrome Type II. Clin Genet. 1985;28(1):54-60. PubMed PMID: 4040823.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Guadalajara camptodactyly syndrome type II. AU - Cantú,J M, AU - García-Cruz,D, AU - Gil-Viera,J, AU - Nazará,Z, AU - Ramírez,M L, AU - Solé-Pujol,M T, AU - Sánchez-Corona,J, PY - 1985/7/1/pubmed PY - 1985/7/1/medline PY - 1985/7/1/entrez SP - 54 EP - 60 JF - Clinical genetics JO - Clin Genet VL - 28 IS - 1 N2 - Two sisters and an unrelated girl presented a distinct intrauterine growth retardation-malformation syndrome with short stature, microcephaly, pectus excavatum, hip dislocation, hypoplastic pubic region and genitalia, camptodactyly, talipes, shortened 2nd toes, hypoplastic patella and skeletal dysplasia probably due to homozygosity from an autosomal recessive gene. SN - 0009-9163 UR - https://www.unboundmedicine.com/medline/citation/4040823/Guadalajara_camptodactyly_syndrome_type_II_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=1985&volume=28&issue=1&spage=54 DB - PRIME DP - Unbound Medicine ER -