[Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients]

Arch Pediatr. 1999:6 Suppl 2:305s-307s. doi: 10.1016/s0929-693x(99)80448-5.

[Article in French]

Authors

G M Brevière¹, M F Croquette, B Delobel, P Pellerin, C Rey

Affiliation

¹ Service des maladies cardiovasculaires infantiles et congénitales, CHRU Lille, France.

PMID: 10370516
DOI: 10.1016/s0929-693x(99)80448-5

No abstract available

MeSH terms

Child
Chromosome Deletion*
Chromosome Mapping
Chromosomes, Human, Pair 22*
Craniofacial Abnormalities / genetics
DiGeorge Syndrome / genetics*
Heart Defects, Congenital / genetics
Humans
Hypocalcemia / genetics
Intellectual Disability / genetics
Psychomotor Performance
Scoliosis / genetics
Thymus Gland / abnormalities*