Deletion 22q11 syndrome: Acknowledging a lost eponym as we say farewell to an acronym [11]

Journal of Medical Genetics

Volumn 38, Issue 4, 2001, Pages 271-272

  Turnpenny, P D ^a   Pigott, R W ^a  

^a ROYAL DEVON AND EXETER HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; FACIES; LETTER; PRIORITY JOURNAL; SOFT PALATE; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLEFT PALATE; DIGEORGE SYNDROME; FACE; HUMANS; SYNDROME; TERMINOLOGY;

EID: 0035058142     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (13)

1. Closing time for CATCH22
2. Molecular characterisation of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation
3. Two 22q telomere deletions serendipitously detected by FISH
4. Insuficience patrohltanového záveru jako vyvojová porucha
5. The syndrome of the congenitally shortened velum. The dual innervation of the soft palate
6. Contribution to knowledge of soft palate innervation
7. Discussions on a new concept of the cellular basis of immunology
8. A new syndrome involving cleft palate, cardiac anomalies, typical facies and learning disabilities: Velo-cardio-facial syndrome
9. Familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphism
10. Etiologic categorization of common congenital heart disease
11. Velopharyngeal (speech) disorder (VP(S)D) without overt cleft palate
12. Syndromes of the head and neck. 3rd ed.
13. Genetic findings in the velofacial (Sedláčková) syndrome