Butler MG - Search Results

1

Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.

Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG. Radhakrishna U, et al. Among authors: butler mg. J Med Genet. 2012 Apr;49(4):270-6. doi: 10.1136/jmedgenet-2012-100826. J Med Genet. 2012. PMID: 22499347 Free PMC article.

2

Screen for MAOA mutations in target human groups.

Schuback DE, Mulligan EL, Sims KB, Tivol EA, Greenberg BD, Chang SF, Yang SL, Mau YC, Shen CY, Ho MS, Yang NH, Butler MG, Fink S, Schwartz CE, Berlin F, Breakefield XO, Murphy DL, Hsu YP. Schuback DE, et al. Among authors: butler mg. Am J Med Genet. 1999 Feb 5;88(1):25-8. Am J Med Genet. 1999. PMID: 10050962 Free PMC article.

3

Trisomy 17 detected in amniotic fluid cells but not in newborn infant.

Butler MG, Neu RL, Mitchell K. Butler MG, et al. Am J Med Genet. 1996 Oct 28;65(3):247-8. doi: 10.1002/ajmg.1320650402. Am J Med Genet. 1996. PMID: 9240752 Free PMC article. No abstract available.

4

Trisomy 18 mosaicism in a 24-year-old white woman with normal intelligence and skeletal abnormalities.

Butler MG. Butler MG. Am J Med Genet. 1994 Oct 15;53(1):92-3. doi: 10.1002/ajmg.1320530124. Am J Med Genet. 1994. PMID: 7802048 Free PMC article. No abstract available.

5

Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

Butler MG, Mowrey P. Butler MG, et al. J Med Genet. 1996 Aug;33(8):719-20. doi: 10.1136/jmg.33.8.719-a. J Med Genet. 1996. PMID: 8863172 Free PMC article. No abstract available.

6

A 26-month-old child with Marden-Walker syndrome and pyloric stenosis.

Gossage D, Perrin JM, Butler MG. Gossage D, et al. Among authors: butler mg. Am J Med Genet. 1987 Apr;26(4):915-9. doi: 10.1002/ajmg.1320260420. Am J Med Genet. 1987. PMID: 3591834 Free PMC article.

7

Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts.

Gripp KW, Johnson C, Scott CI Jr, Nicholson L, Bober M, Butler MG, Shaw L, Gorlin RJ. Gripp KW, et al. Among authors: butler mg. Am J Med Genet A. 2008 Feb 15;146A(4):468-73. doi: 10.1002/ajmg.a.32155. Am J Med Genet A. 2008. PMID: 18203204 Free PMC article. Review.

8

Marshall-Smith syndrome: Follow-up report of a four and a half year old male.

Butler MG. Butler MG. Am J Med Genet A. 2004 Apr 30;126A(3):329-30. doi: 10.1002/ajmg.a.20603. Am J Med Genet A. 2004. PMID: 15054853 Free PMC article. No abstract available.

9

Genetics of Prader-Willi and Angelman syndromes: 2024 update.

Godler DE, Singh D, Butler MG. Godler DE, et al. Among authors: butler mg. Curr Opin Psychiatry. 2024 Dec 19. doi: 10.1097/YCO.0000000000000981. Online ahead of print. Curr Opin Psychiatry. 2024. PMID: 39804213

10

Six at Sixty. Commentary on identification of the PTEN gene as a major contributor to autism spectrum disorder.

Butler MG. Butler MG. J Med Genet. 2024 Dec 31;62(1):48-52. doi: 10.1136/jmg-2024-110470. J Med Genet. 2024. PMID: 39643434 No abstract available.

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