Autor:	L, Lambie, T J, de Ravel
Rok vydání:	2000
Předmět:	Male Cytogenetics South Africa Langer-Giedion Syndrome Child Preschool Mutation Humans Genetic Counseling Prognosis Gene Deletion
Zdroj:	East African medical journal. 77(1)
ISSN:	0012-835X
Popis:	Patients with the trichorhinophalangeal syndrome type II, also known as the Langer-Giedion syndrome, may present to the health care-givers or physicians in various specialties and need to be recognised in order that accurate diagnosis, management and counselling about prognosis and recurrence risks may be carried out. A case of young male with this condition is presented.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::1c73f9876636bb16ddbf9ff8b1652cc3 https://pubmed.ncbi.nlm.nih.gov/10944842 Zobrazit plný text záznamu