History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype? | Clin Dysmorphol;21(2): 97-100, 2012 Apr. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Advanced Search EVID@Easy

History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?

Jezela-Stanek, Aleksandra; Kucharczyk, Marzena; Gutkowska, Anna; Pelc, Magdalena; Ciara, Elzbieta; Chrzanowska, Krystyna H; Krajewska-Walasek, Malgorzata.

Affiliation

Jezela-Stanek A; Department of Medical Genetics, The Children's Memorial Health Institute, Warsaw, Poland.

Clin Dysmorphol ; 21(2): 97-100, 2012 Apr.

Article in En | MEDLINE | ID: mdl-22391620

Subject(s)

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 14 / Chromosome Deletion / Chromosome Disorders Limits: Female / Humans / Infant Language: En Journal: Clin Dysmorphol Journal subject: TERATOLOGIA Year: 2012 Document type: Article Affiliation country: Country of publication:

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 14 / Chromosome Deletion / Chromosome Disorders Limits: Female / Humans / Infant Language: En Journal: Clin Dysmorphol Journal subject: TERATOLOGIA Year: 2012 Document type: Article Affiliation country: Country of publication: