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2. The Williams syndrome: evidence for possible autosomal dominant inheritance. Sadler LS; Robinson LK; Verdaasdonk KR; Gingell R Am J Med Genet; 1993 Sep; 47(4):468-70. PubMed ID: 8256806 [TBL] [Abstract][Full Text] [Related]
3. Williams syndrome in one dizygotic twin. Hokama T; Rogers JG Acta Paediatr Jpn; 1991 Oct; 33(5):678-80. PubMed ID: 1799126 [TBL] [Abstract][Full Text] [Related]
4. Williams syndrome: autosomal dominant inheritance. Morris CA; Thomas IT; Greenberg F Am J Med Genet; 1993 Sep; 47(4):478-81. PubMed ID: 8256809 [TBL] [Abstract][Full Text] [Related]
6. [Familial occurrence of Elfin's face (Williams-Beurens Syndrome =wbs) and supravalvular aortic stenosis (= svas) (author's transl)]. Hammerer I; Gassner I; Müller W Klin Padiatr; 1979 May; 191(3):287-92. PubMed ID: 572446 [TBL] [Abstract][Full Text] [Related]
7. Williams-Beuren syndrome in monozygotic twins with variable expression. Pankau R; Gosch A; Simeoni E; Wessel A Am J Med Genet; 1993 Sep; 47(4):475-7. PubMed ID: 8256808 [TBL] [Abstract][Full Text] [Related]
8. Familial aggregation of defects of the left-sided structures of the heart. Menahem S Int J Cardiol; 1990 Nov; 29(2):239-40. PubMed ID: 2269543 [TBL] [Abstract][Full Text] [Related]
9. An operated case of Holt-Oram syndrome with autosomal dominant inheritance. Czakó Z; Gömöry A; Homolay P; Bacsa S; Kiss S; Móricz F; Fülöp F; Papp Z Basic Res Cardiol; 1976; 71(1):60-7. PubMed ID: 1259686 [TBL] [Abstract][Full Text] [Related]
10. Cardio-cutaneous syndrome (the "LEOPARD" syndrome). Review of the literature and a new family. Seuanez H; Mañe-Garzon F; Kolski R Clin Genet; 1976 Mar; 9(3):266-76. PubMed ID: 1261064 [TBL] [Abstract][Full Text] [Related]
11. Concurrence of supravalvular aortic stenosis and peripheral pulmonary stenosis in three generations of a family: a form of arterial dysplasia. Kumar A; Stalker HJ; Williams CA Am J Med Genet; 1993 Mar; 45(6):739-42. PubMed ID: 8456853 [TBL] [Abstract][Full Text] [Related]
12. A monozygotic twin pregnancy discordant for acardia and X-inactivation pattern. Masuzaki H; Miura K; Yoshimura S; Yoshiura K; Ishimaru T Eur J Obstet Gynecol Reprod Biol; 2004 Nov; 117(1):102-4. PubMed ID: 15474253 [TBL] [Abstract][Full Text] [Related]
13. Concordance and discordance of congenital heart disease in 20 families. Davison BC J Med Genet; 1967 Dec; 4(4):245-50. PubMed ID: 6082900 [No Abstract] [Full Text] [Related]
14. Malformations unique to the twinning process. Nance WE Prog Clin Biol Res; 1981; 69A():123-33. PubMed ID: 7029570 [No Abstract] [Full Text] [Related]
15. [Familial supravalvular aortic stenosis. Investigation in a family and review of the literature]. Burnel P; Marçon F; Lucron H; Bosser G; Gilgenkrantz S; Jonveaux P; Chéry M; Worms AM Arch Mal Coeur Vaiss; 1997 May; 90(5):719-24. PubMed ID: 9295957 [TBL] [Abstract][Full Text] [Related]
16. Twins and their mildly affected mother with Weaver syndrome. Dumić M; Vuković J; Cvitkovic M; Medica I Clin Genet; 1993 Dec; 44(6):338-40. PubMed ID: 8131308 [TBL] [Abstract][Full Text] [Related]
17. Autosomal recessive type of whistling face syndrome in twins. Kousseff BG; McConnachie P; Hadro TA Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706 [TBL] [Abstract][Full Text] [Related]
18. Williams syndrome in twins. Murphy MB; Greenberg F; Wilson G; Hughes M; DiLiberti J Am J Med Genet Suppl; 1990; 6():97-9. PubMed ID: 2118786 [TBL] [Abstract][Full Text] [Related]
19. [The use of Doty's extended aortoplasty in binovular twins with congenital supravalvular aortic stenosis]. Tedoriya T; Kawasuji M; Sakakibara N; Hirano K; Watanabe Y; Iwa T Nihon Kyobu Geka Gakkai Zasshi; 1991 Nov; 39(11):2092-5. PubMed ID: 1774493 [TBL] [Abstract][Full Text] [Related]
20. A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton. Stevenson RE; Taylor HA; Burton OM; Hearn HB J Med Genet; 1980 Jun; 17(3):238-42. PubMed ID: 7401139 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]