Catalogo Articoli (Spogli Riviste)

OPAC HELP

Titolo:
Robinow syndrome in monozygotic twins with normal stature
Autore:
Saraiva, JM; Cordeiro, I; Santos, HG;
Indirizzi:
Hosp Pediat Coimbra, Consulta Genet, P-3000 Coimbra, Portugal Hosp Pediat Coimbra Coimbra Portugal P-3000 et, P-3000 Coimbra, Portugal Hosp Santa Maria, Serv Pediat, Unidade Genet, Lisbon, Portugal Hosp Santa Maria Lisbon Portugal ediat, Unidade Genet, Lisbon, Portugal
Titolo Testata:
CLINICAL DYSMORPHOLOGY
fascicolo: 2, volume: 8, anno: 1999,
pagine: 147 - 150
SICI:
0962-8827(199904)8:2<147:RSIMTW>2.0.ZU;2-P
Fonte:
ISI
Lingua:
ENG
Keywords:
fetal face; omphalocele; Robinow syndrome;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
12
Recensione:
Indirizzi per estratti:
Indirizzo: Saraiva, JM Hosportugal Coimbra, Consulta Genet, Ave Bissaya Barreto, P-3000 Coimbra, P Hosp Pediat Coimbra Ave Bissaya Barreto Coimbra Portugal P-3000
Citazione:
J.M. Saraiva et al., "Robinow syndrome in monozygotic twins with normal stature", CLIN DYSMOR, 8(2), 1999, pp. 147-150

Abstract

Robinow syndrome was found in two monozygotic twins. We describe the clinical and radiographic manifestations in these patients, both with normal stature and one with omphalocele, with a follow-up of 13 years. Families with Robinow syndrome of both autosomal dominant and recessive inheritance have been reported. We apply the criteria suggested to assign isolated cases to one of the two forms and conclude that autosomal dominant inheritance is more likely. Clin Dysmorphol 8: 147-150 (C) 1999 Lippincott Williams & Wilkins.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/09/20 alle ore 05:25:52