Le diagnostic prénatal des maladies génétiques: expérience lausannoise 1989-1993 [Prenatal diagnosis of genetic diseases: Lausanne experience 1989-1993]

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Autoria(s): Fokstuen S.; Pescia G.; Addor M.C.; Gaide A.C.; Marguerat P.; Maillard C.; Vial Y.; Hohlfeld P.; Nguyen The H.

Data(s)	1994
Identificador	http://serval.unil.ch/?id=serval:BIB_73A70EE593DA isbn:0035-3655 pmid:7817068
Idioma(s)	fr
Fonte	Revue Médicale de la Suisse Romande, vol. 114, no. 12, pp. 1055-1065
Palavras-Chave	#Amniotic Fluid; Chorionic Villi Sampling; Chromosome Aberrations; Chromosome Disorders; Cytogenetics; Down Syndrome; Female; Genetic Counseling; Gestational Age; Humans; Infant, Newborn; Pregnancy; Prenatal Diagnosis; Specimen Handling; Switzerland; Ultrasonography, Prenatal
Tipo	info:eu-repo/semantics/review article