Interstitial deletion 6p22.3-p24.3 characterized by CGH array in a foetus with multiple malformations

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Bibliographic Details
Published in:Prenatal diagnosis 2009-09, Vol.29 (9), p.908-910
Main Authors: Colmant, C., Brisset, S., Tachdjian, G., Gautier, V., Ftouki, M., Laroudie, M., Druart, L., Frydman, R., Picone, O.
Format: Article
Language:English
Subjects:
Abnormalities, Multiple - diagnosis
Abnormalities, Multiple - genetics
Abnormalities, Multiple - pathology
Adult
array CGH
Biological and medical sciences
Chromosome Deletion
Chromosomes, Human, Pair 6
Comparative Genomic Hybridization - methods
del6p
Delivery. Postpartum. Lactation
Female
fetal ultrasound
Fetus - metabolism
Fetus - pathology
foetal imaging
Fundamental and applied biological sciences. Psychology
genetic counselling
Genetics of eukaryotes. Biological and molecular evolution
Gynecology. Andrology. Obstetrics
Humans
Medical sciences
Molecular and cellular biology
Oligonucleotide Array Sequence Analysis - methods
Polycystic Kidney Diseases - complications
Polycystic Kidney Diseases - diagnosis
Pregnancy
prenatal cytogenetics
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ISSN:0197-3851
1097-0223
DOI:10.1002/pd.2306