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1959 2
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1966 7
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1968 8
1969 5
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1971 10
1972 2
1973 2
1974 1
1975 1
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1977 8
1978 3
1979 6
1980 7
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1983 15
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1986 5
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1988 10
1989 17
1990 14
1991 10
1992 14
1993 39
1994 25
1995 11
1996 13
1997 9
1998 18
1999 6
2000 15
2001 13
2002 7
2003 19
2004 16
2005 12
2006 20
2007 22
2008 19
2009 32
2010 29
2011 36
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1,031 results

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Page 1
Brachmann-de Lange syndrome with normal IQ.
Saal HM, Samango-Sprouse CA, Rodnan LA, Rosenbaum KN, Custer DA. Saal HM, et al. Am J Med Genet. 1993 Nov 15;47(7):995-8. doi: 10.1002/ajmg.1320470711. Am J Med Genet. 1993. PMID: 8291543 Review.
The Brachmann-de Lange syndrome is a disorder with a high degree of clinical variability, generally associated with moderate to severe mental retardation. To date, 7 previous cases of Brachmann-de Lange syndrome with normal intelligence (IQ > 70) have been descri …
The Brachmann-de Lange syndrome is a disorder with a high degree of clinical variability, generally associated with moderate to sever …
The Brachmann-de Lange syndrome.
Opitz JM. Opitz JM. Am J Med Genet. 1985 Sep;22(1):89-102. doi: 10.1002/ajmg.1320220110. Am J Med Genet. 1985. PMID: 3901753 Review. No abstract available.
BRACHMANN/DE LANGE SYNDROME.
OPITZ JM, SEGAL AT, LEHRKE R, NADLER H. OPITZ JM, et al. Lancet. 1964 Nov 7;2(7367):1019. doi: 10.1016/s0140-6736(64)90980-8. Lancet. 1964. PMID: 14201663 No abstract available.
Brachmann-de Lange syndrome. 1994 update.
Kousseff BG, Newkirk P, Root AW. Kousseff BG, et al. Arch Pediatr Adolesc Med. 1994 Jul;148(7):749-55. doi: 10.1001/archpedi.1994.02170070087016. Arch Pediatr Adolesc Med. 1994. PMID: 8019632 Review.
OBJECTIVE: To update the phenotype, cause, mode of inheritance, and certainty of the diagnosis of Brachmann-de Lange syndrome. DESIGN: Case series with comparative review of pertinent literature. SETTING: A tertiary university-based pediatric genetic clinic. PARTICIPANTS: …
OBJECTIVE: To update the phenotype, cause, mode of inheritance, and certainty of the diagnosis of Brachmann-de Lange syndrome. DESIGN …
Aniridia and Brachmann-de Lange syndrome: a review of ocular surface and anterior segment findings.
Lee WB, Brandt JD, Mannis MJ, Huang CQ, Rabin GJ. Lee WB, et al. Cornea. 2003 Mar;22(2):178-80. doi: 10.1097/00003226-200303000-00021. Cornea. 2003. PMID: 12605058 Review.
Aniridia and congenital glaucoma were not previously reported with Brachmann-de Lange syndrome. CONCLUSIONS: Ocular surface and anterior segment abnormalities must be considered when examining patients with Brachmann-de Lange syndrome. ...To our knowledge, these fin …
Aniridia and congenital glaucoma were not previously reported with Brachmann-de Lange syndrome. CONCLUSIONS: Ocular surface and anter …
[Brachmann-de Lange syndrome].
Tsukahara M. Tsukahara M. Ryoikibetsu Shokogun Shirizu. 2001;(33):299-301. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462447 Review. Japanese. No abstract available.
A further report of Brachmann-de Lange syndrome in two sibs with normal parents.
Krajewska-Walasek M, Chrzanowska K, Tylki-Szymańska A, Białecka M. Krajewska-Walasek M, et al. Clin Genet. 1995 Jun;47(6):324-7. doi: 10.1111/j.1399-0004.1995.tb03974.x. Clin Genet. 1995. PMID: 7554368 Review.
We report on a family in which a girl and a boy in the same sibship show variable manifestations of a less severe type of Brachmann-de Lange syndrome without significant prenatal growth deficiency and reduction deformities of the forearms. ...All the affected sibs except o …
We report on a family in which a girl and a boy in the same sibship show variable manifestations of a less severe type of Brachmann-d …
Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature.
Feingold M, Lin AE. Feingold M, et al. Am J Med Genet. 1993 Nov 15;47(7):1064-7. doi: 10.1002/ajmg.1320470726. Am J Med Genet. 1993. PMID: 8291524 Review.
We report on a mother and daughter with the Brachmann-de Lange syndrome which supports the view that in some families this disorder is due to autosomal dominant inheritance. ...
We report on a mother and daughter with the Brachmann-de Lange syndrome which supports the view that in some families this disorder i …
Effect of MRI-Guided Fibrosis Ablation vs Conventional Catheter Ablation on Atrial Arrhythmia Recurrence in Patients With Persistent Atrial Fibrillation: The DECAAF II Randomized Clinical Trial.
Marrouche NF, Wazni O, McGann C, Greene T, Dean JM, Dagher L, Kholmovski E, Mansour M, Marchlinski F, Wilber D, Hindricks G, Mahnkopf C, Wells D, Jais P, Sanders P, Brachmann J, Bax JJ, Morrison-de Boer L, Deneke T, Calkins H, Sohns C, Akoum N; DECAAF II Investigators. Marrouche NF, et al. JAMA. 2022 Jun 21;327(23):2296-2305. doi: 10.1001/jama.2022.8831. JAMA. 2022. PMID: 35727277 Free PMC article. Clinical Trial.
Radiological features in Brachmann-de Lange syndrome.
Braddock SR, Lachman RS, Stoppenhagen CC, Carey JC, Ireland M, Moeschler JB, Cunniff C, Graham JM Jr. Braddock SR, et al. Am J Med Genet. 1993 Nov 15;47(7):1006-13. doi: 10.1002/ajmg.1320470714. Am J Med Genet. 1993. PMID: 8291513 Review.
Brachmann-de Lange syndrome (BDLS) is a well-delineated disorder consisting variably of pre- and postnatal growth deficiency, microbrachycephaly, characteristic face, hypertrichosis, visceral anomalies, and limb defects consisting primarily of variable limb reduction defec …
Brachmann-de Lange syndrome (BDLS) is a well-delineated disorder consisting variably of pre- and postnatal growth deficiency, microbr …
1,031 results