1.
J Pediatr
; 92(3): 446-8, 1978 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-632988
2.
J Med Genet
; 14(3): 214-8, 1977 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-881715
RESUMO
A liveborn infant with the complement 46,XX/47,XX, + 14 shared certain features in common with the following previously reported cases: (1) the one previously reported possible case of trisomy 14, (2) cases in which individuals had at least some portion of chromosome No. 14 in triplicate, and (3) cases of atypical D trisomy (Snodgrass category II). The common features include developmental retardation, wide flat nose with bulbous or wide tip, large mouth with turned down corners (some with protruding lips), short neck (some with redundant skin folds), low-set ears, retrognathia, digital anomalies (usually contractions and deviations), palatal anomalies, and cryptorchidism.
Assuntos
Cromossomos Humanos 13-15 , Mosaicismo , Trissomia , Desenvolvimento Infantil , Aberrações Cromossômicas/genética , Transtornos Cromossômicos , Face , Feminino , Humanos , Lactente , Recém-Nascido
3.
J Med Genet
; 11(4): 367-70, 1974 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-4443985