Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome. [electronic resource]
Producer: 20060307Description: 17-23 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Chromosome Deletion
- Chromosomes, Human, Pair 1 -- genetics
- Cleft Palate -- pathology
- Craniofacial Abnormalities -- pathology
- Fatal Outcome
- Genetic Predisposition to Disease -- genetics
- Genome, Human
- Hernia, Diaphragmatic -- genetics
- Hernias, Diaphragmatic, Congenital
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Karyotyping
- Limb Deformities, Congenital -- pathology
- Nails, Malformed
- Nucleic Acid Hybridization -- methods
- Syndrome
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, N.I.H., Extramural
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