1.
Eur J Pediatr
; 143(3): 233-5, 1985 Jan.
Article
in English
| MEDLINE
| ID: mdl-3987723
ABSTRACT
Two boys and two girls from a sibship of six, affected with the Wiedemann-Beckwith syndrome (WBS), are reported. One of the patients also had congenital hypothyroidism, an association hitherto undescribed and possibly fortuitous. Neither stigmata of WBS in other family members nor parental consanguinity were found, indicating a possible autosomal dominant inheritance comprising either a delayed mutation of an unstable premutated gene or non-penetrance.
Subject(s)
Beckwith-Wiedemann Syndrome/genetics , Congenital Hypothyroidism , Child, Preschool , Female , Hernia, Umbilical/genetics , Humans , Hypothyroidism/complications , Infant , Macroglossia/genetics , Male , Pedigree
2.
Rev Clin Esp
; 161(5-6): 343-6, 1981.
Article
in Spanish
| MEDLINE
| ID: mdl-7291649
3.
Ginecol Obstet Mex
; 48(287): 159-69, 1980 Sep.
Article
in Spanish
| MEDLINE
| ID: mdl-7203096
4.
Ginecol Obstet Mex
; 45(272): 463-6, 1979 Jun.
Article
in Spanish
| MEDLINE
| ID: mdl-89062
Subject(s)
Anencephaly , Hydatidiform Mole , Adult , Chorionic Gonadotropin/blood , Female , Fetal Blood , Fetal Death , Humans , Pregnancy , Sex Factors , alpha-Fetoproteins/blood
5.
Arch Inst Cardiol Mex
; 44(4): 652-60, 1974.
Article
in Spanish
| MEDLINE
| ID: mdl-4859063