These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
110 related articles for article (PubMed ID: 3799716)
1. Familial occurrence of Brachmann-de Lange syndrome. Bankier A; Haan E; Birrell R Am J Med Genet; 1986 Sep; 25(1):163-5. PubMed ID: 3799716 [No Abstract] [Full Text] [Related]
2. Brachmann-de Lange syndrome: autosomal dominant inheritance and male-to-male transmission. McKenney RR; Elder FF; Garcia J; Northrup H Am J Med Genet; 1996 Dec; 66(4):449-52. PubMed ID: 8989466 [TBL] [Abstract][Full Text] [Related]
3. Male-to-male transmission of mild Brachmann-de Lange syndrome. Chodirker BN; Chudley AE Am J Med Genet; 1994 Sep; 52(3):331-3. PubMed ID: 7528973 [TBL] [Abstract][Full Text] [Related]
4. Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature. Feingold M; Lin AE Am J Med Genet; 1993 Nov; 47(7):1064-7. PubMed ID: 8291524 [TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant inheritance of Brachmann-de Lange syndrome. Kozma C Am J Med Genet; 1996 Dec; 66(4):445-8. PubMed ID: 8989465 [TBL] [Abstract][Full Text] [Related]
6. Brachmann-de Lange syndrome: evidence for autosomal dominant inheritance. Robinson LK; Wolfsberg E; Jones KL Am J Med Genet; 1985 Sep; 22(1):109-15. PubMed ID: 4050846 [TBL] [Abstract][Full Text] [Related]
7. Exclusively maternal transmission of autosomal dominant Brachmann-de Lange syndrome. de Die-Smulders C; Schrander-Stumpel C; Fryns JP; Theunissen P Am J Med Genet; 1994 Sep; 52(3):363. PubMed ID: 7810572 [No Abstract] [Full Text] [Related]
8. An analysis of seven infants with Brachmann-de Lange syndrome, of whom two identical twin sisters. Caksen H; Kurtoğlu S; Cesur Y; Oztürk A Genet Couns; 2001; 12(4):373-7. PubMed ID: 11837608 [TBL] [Abstract][Full Text] [Related]
9. Congenital diaphragmatic hernia in the Brachmann-de Lange syndrome. Cunniff C; Curry CJ; Carey JC; Graham JM; Williams CA; Stengel-Rutkowski S; Lüttgen S; Meinecke P Am J Med Genet; 1993 Nov; 47(7):1018-21. PubMed ID: 8291515 [TBL] [Abstract][Full Text] [Related]
10. Brachmann-de Lange syndrome with normal IQ. Saal HM; Samango-Sprouse CA; Rodnan LA; Rosenbaum KN; Custer DA Am J Med Genet; 1993 Nov; 47(7):995-8. PubMed ID: 8291543 [TBL] [Abstract][Full Text] [Related]
11. No uniparental disomy for chromosome 3 in Brachmann-De Lange syndrome. De Marchi N; Antonarakis SE; Jackson L Am J Med Genet; 1994 Jan; 49(1):133-5. PubMed ID: 8172242 [No Abstract] [Full Text] [Related]
12. Mild Brachmann-de Lange syndrome: changes of phenotype with age. Greenberg F; Robinson LK Am J Med Genet; 1989 Jan; 32(1):90-2. PubMed ID: 2705489 [TBL] [Abstract][Full Text] [Related]
13. [The Brachmann-De Lange syndrome. Presentation of a case. Clinical and etiological discussion]. Castello M; Parisi P; Turlà B Clin Pediatr (Bologna); 1966 Dec; 48(12):627-43. PubMed ID: 5998215 [No Abstract] [Full Text] [Related]
14. Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome. Breslau EJ; Disteche C; Hall JG; Thuline H; Cooper P Am J Med Genet; 1981; 10(2):179-86. PubMed ID: 7315874 [TBL] [Abstract][Full Text] [Related]
16. Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation. Hosokawa S; Takahashi N; Kitajima H; Nakayama M; Kosaki K; Okamoto N Congenit Anom (Kyoto); 2010 Jun; 50(2):129-32. PubMed ID: 20156239 [TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 4p and Brachmann-de Lange syndrome. Fryns JP Am J Med Genet; 2000 Dec; 95(4):406. PubMed ID: 11186901 [No Abstract] [Full Text] [Related]
18. The Brachmann-de Lange syndrome. Opitz JM Am J Med Genet; 1985 Sep; 22(1):89-102. PubMed ID: 3901753 [No Abstract] [Full Text] [Related]
19. Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotype. Saul RA; Rogers RC; Phelan MC; Stevenson RE Am J Med Genet; 1993 Nov; 47(7):999-1002. PubMed ID: 8291544 [TBL] [Abstract][Full Text] [Related]
20. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype. Lopez-Rangel E; Dill FJ; Hrynchak MA; Van Allen MI Am J Med Genet; 1993 Nov; 47(7):1068-71. PubMed ID: 8291525 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]