Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.Birth Defects Orig Artic Ser. 1976; 12(5):201-8.BD
MeSH
Pub Type(s)
Case Reports
Journal Article
Language
eng
PubMed ID
953225
Citation
Pena, S D., and M H. Shokeir. "Syndrome of Camptodactyly, Multiple Ankyloses, Facial Anomalies and Pulmonary Hypoplasia--further Delineation and Evidence for Autosomal Recessive Inheritance." Birth Defects Original Article Series, vol. 12, no. 5, 1976, pp. 201-8.
Pena SD, Shokeir MH. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance. Birth Defects Orig Artic Ser. 1976;12(5):201-8.
Pena, S. D., & Shokeir, M. H. (1976). Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance. Birth Defects Original Article Series, 12(5), 201-8.
Pena SD, Shokeir MH. Syndrome of Camptodactyly, Multiple Ankyloses, Facial Anomalies and Pulmonary Hypoplasia--further Delineation and Evidence for Autosomal Recessive Inheritance. Birth Defects Orig Artic Ser. 1976;12(5):201-8. PubMed PMID: 953225.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
AU - Pena,S D,
AU - Shokeir,M H,
PY - 1976/1/1/pubmed
PY - 1976/1/1/medline
PY - 1976/1/1/entrez
SP - 201
EP - 8
JF - Birth defects original article series
JO - Birth Defects Orig Artic Ser
VL - 12
IS - 5
SN - 0547-6844
UR - https://www.unboundmedicine.com/medline/citation/953225/Syndrome_of_camptodactyly_multiple_ankyloses_facial_anomalies_and_pulmonary_hypoplasia__further_delineation_and_evidence_for_autosomal_recessive_inheritance_
DB - PRIME
DP - Unbound Medicine
ER -