Teebi hypertelorism syndrome: report of a third family.Clin Dysmorphol. 1994 Oct; 3(4):335-9.CD
Abstract
We report a mother and daughter who have hypertelorism, mild limb defects, umbilical hernia/omphalocele, natal teeth and minor craniofacial anomalies. These individuals represent the third family with Teebi hypertelorism syndrome, a rare autosomal dominant syndrome.
Links
MeSH
Pub Type(s)
Case Reports
Journal Article
Review
Language
eng
PubMed ID
7894738
Citation
Toriello, H V., and K Delp. "Teebi Hypertelorism Syndrome: Report of a Third Family." Clinical Dysmorphology, vol. 3, no. 4, 1994, pp. 335-9.
Toriello HV, Delp K. Teebi hypertelorism syndrome: report of a third family. Clin Dysmorphol. 1994;3(4):335-9.
Toriello, H. V., & Delp, K. (1994). Teebi hypertelorism syndrome: report of a third family. Clinical Dysmorphology, 3(4), 335-9.
Toriello HV, Delp K. Teebi Hypertelorism Syndrome: Report of a Third Family. Clin Dysmorphol. 1994;3(4):335-9. PubMed PMID: 7894738.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Teebi hypertelorism syndrome: report of a third family.
AU - Toriello,H V,
AU - Delp,K,
PY - 1994/10/1/pubmed
PY - 1994/10/1/medline
PY - 1994/10/1/entrez
SP - 335
EP - 9
JF - Clinical dysmorphology
JO - Clin Dysmorphol
VL - 3
IS - 4
N2 - We report a mother and daughter who have hypertelorism, mild limb defects, umbilical hernia/omphalocele, natal teeth and minor craniofacial anomalies. These individuals represent the third family with Teebi hypertelorism syndrome, a rare autosomal dominant syndrome.
SN - 0962-8827
UR - https://www.unboundmedicine.com/medline/citation/7894738/Teebi_hypertelorism_syndrome:_report_of_a_third_family_
L2 - http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE=linkout&SEARCH=7894738.ui
DB - PRIME
DP - Unbound Medicine
ER -