Results 151 to 160 of about 3,948 (205)

Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasia. [PDF]

Medicine (Baltimore), 2021
Yang L, Lu G, Shen W, Chen W, Lu H, Zhang G, Yuan S, Zheng S, Ren J.   +8 more
europepmc   +1 more source

Clinical and Radiological Insights of Cleidocranial Dysplasia: A Case Report of a Rare Medical Condition. [PDF]

Cureus
Gowda Venkatesha RR, Rajaram Mohan K, Aravind M, Sridharrao V, Rajalingam S.   +4 more
europepmc   +1 more source

Familial Cleidocranial Dysplasia: A Diagnostic Challenge. [PDF]

Indian J Otolaryngol Head Neck Surg
Verma S, Koppula S, Kumar V.
europepmc   +1 more source

Cleidocranial Dysplasia Presenting With Mixed Dentition in a 28-Year-Old Male: A Case Report. [PDF]

Cureus
Gollapudi M, Mohod S, Mahajan NR, Tiwari AV.   +3 more
europepmc   +1 more source

New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia. [PDF]

Biology (Basel)
Toral López J, Gómez Martinez S, Rivera Vega MDR, Hernández-Zamora E, Cuevas Covarrubias S, Ibarra Castrejón BA, González Huerta LM.   +6 more
europepmc   +1 more source

A Rare Case of Cleidocranial Dysplasia Causing Unilateral Lung Herniation in the Setting of an Acute Viral Infection. [PDF]

Cureus
Ghias M, Bogdansky K, Murray D, Sunzeri L, Arevalo Marcano C.   +4 more
europepmc   +1 more source

Prenatal diagnosis of cleidocranial dysplasia: Case report on two cases with a negative family history. [PDF]

Heliyon
Han R, Zhang C, Fu X, Zhu Z, Wang X, Li H.   +5 more
europepmc   +1 more source

Prenatal ultrasonography and genetic analysis of fetal cleidocranial dysplasia: A case report.

World J Clin Cases
Wang F, Dai PF, Gao WJ.
europepmc   +1 more source

Cleidocranial dysplasia.

Indian pediatrics, 1996
A, Sharma, R, Yadav, K, Ahlawat
openaire   +1 more source

Cleidocranial dysplasia.

Indian pediatrics, 2004
Archana B, Patel, Ambarish M, Athavale
openaire   +1 more source