Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1982 1
1985 4
1986 6
1987 7
1988 3
1989 5
1990 1
1991 5
1992 8
1993 5
1994 7
1995 3
1996 3
1997 8
1998 3
1999 7
2000 11
2001 7
2002 7
2003 6
2004 9
2005 8
2006 4
2007 5
2008 8
2009 6
2010 4
2011 1
2012 2
2013 3
2014 3
2015 3
2016 1
2017 5
2019 1
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

164 results

Results by year

Filters applied: . Clear all
Page 1
Robinow syndrome.
Patton MA, Afzal AR. Patton MA, et al. J Med Genet. 2002 May;39(5):305-10. doi: 10.1136/jmg.39.5.305. J Med Genet. 2002. PMID: 12011143 Free PMC article. Review.
Russell-Silver syndrome.
Patton MA. Patton MA. J Med Genet. 1988 Aug;25(8):557-60. doi: 10.1136/jmg.25.8.557. J Med Genet. 1988. PMID: 3050100 Free PMC article. Review. No abstract available.
Floating-Harbor syndrome.
Patton MA, Hurst J, Donnai D, McKeown CM, Cole T, Goodship J. Patton MA, et al. J Med Genet. 1991 Mar;28(3):201-4. doi: 10.1136/jmg.28.3.201. J Med Genet. 1991. PMID: 2051457 Free PMC article. No abstract available.
Genetic studies in the Amish community.
Patton MA. Patton MA. Ann Hum Biol. 2005 Mar-Apr;32(2):163-7. doi: 10.1080/03014460500075274. Ann Hum Biol. 2005. PMID: 16096212 Review.
Genetic aspects of congenital malformations.
Patton MA. Patton MA. Baillieres Clin Obstet Gynaecol. 1987 Sep;1(3):723-35. doi: 10.1016/s0950-3552(87)80013-5. Baillieres Clin Obstet Gynaecol. 1987. PMID: 3325212 Review.
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
Ion A, Tartaglia M, Song X, Kalidas K, van der Burgt I, Shaw AC, Ming JE, Zampino G, Zackai EH, Dean JC, Somer M, Parenti G, Crosby AH, Patton MA, Gelb BD, Jeffery S. Ion A, et al. Among authors: patton ma. Hum Genet. 2002 Oct;111(4-5):421-7. doi: 10.1007/s00439-002-0803-6. Epub 2002 Aug 24. Hum Genet. 2002. PMID: 12384786 Review.
The Aase-Smith syndrome.
Patton MA, Sharma A, Winter RM. Patton MA, et al. Clin Genet. 1985 Dec;28(6):521-5. doi: 10.1111/j.1399-0004.1985.tb00420.x. Clin Genet. 1985. PMID: 4075562
Hearing impairment in 18q deletion syndrome.
Jayarajan V, Swan IR, Patton MA. Jayarajan V, et al. Among authors: patton ma. J Laryngol Otol. 2000 Dec;114(12):963-6. doi: 10.1258/0022215001904473. J Laryngol Otol. 2000. PMID: 11177369 Review.
Eusol: the continuing controversy.
Patton MA. Patton MA. BMJ. 1992 Jun 20;304(6842):1636. doi: 10.1136/bmj.304.6842.1636-a. BMJ. 1992. PMID: 1628106 Free PMC article. No abstract available.
164 results