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

Text availability

Article attribute

Article type

Publication date

Search Results

123 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide.
Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Renlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick OM, López MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martínez-Frías ML, Gallagher M, Erickson JD, Vollset SE, Mastroiacovo P, Andria G, Botto LD. Wilcken B, et al. Among authors: mutchinick om. J Med Genet. 2003 Aug;40(8):619-25. doi: 10.1136/jmg.40.8.619. J Med Genet. 2003. PMID: 12920077 Free PMC article. No abstract available.
A joint international study on the epidemiology of hypospadias.
Källén B, Bertollini R, Castilla E, Czeizel A, Knudsen LB, Martinez-Frias ML, Mastroiacovo P, Mutchinick O. Källén B, et al. Acta Paediatr Scand Suppl. 1986;324:1-52. doi: 10.1111/j.1651-2227.1986.tb14935.x. Acta Paediatr Scand Suppl. 1986. PMID: 3471045
The spectrum of congenital anomalies of the VATER association: an international study.
Botto LD, Khoury MJ, Mastroiacovo P, Castilla EE, Moore CA, Skjaerven R, Mutchinick OM, Borman B, Cocchi G, Czeizel AE, Goujard J, Irgens LM, Lancaster PA, Martínez-Frías ML, Merlob P, Ruusinen A, Stoll C, Sumiyoshi Y. Botto LD, et al. Among authors: mutchinick om. Am J Med Genet. 1997 Jul 11;71(1):8-15. doi: 10.1002/(sici)1096-8628(19970711)71:1<8::aid-ajmg2>3.0.co;2-v. Am J Med Genet. 1997. PMID: 9215761
Congenital malformations in twins: an international study.
Mastroiacovo P, Castilla EE, Arpino C, Botting B, Cocchi G, Goujard J, Marinacci C, Merlob P, Métneki J, Mutchinick O, Ritvanen A, Rosano A. Mastroiacovo P, et al. Am J Med Genet. 1999 Mar 12;83(2):117-24. doi: 10.1002/(sici)1096-8628(19990312)83:2<117::aid-ajmg7>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10190482
Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems.
Rosano A, Botto LD, Olney RS, Khoury MJ, Ritvanen A, Goujard J, Stoll C, Cocchi G, Merlob P, Mutchinick O, Cornel MC, Castilla EE, Martínez-Frías ML, Zampino G, Erickson JD, Mastroiacovo P. Rosano A, et al. Am J Med Genet. 2000 Jul 17;93(2):110-6. doi: 10.1002/1096-8628(20000717)93:2<110::aid-ajmg6>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10869112
Sex and congenital malformations: an international perspective.
Lisi A, Botto LD, Rittler M, Castilla E, Bianca S, Bianchi F, Botting B, De Walle H, Erickson JD, Gatt M, De Vigan C, Irgens L, Johnson W, Lancaster P, Merlob P, Mutchinick OM, Ritvanen A, Robert E, Scarano G, Stoll C, Mastroiacovo P. Lisi A, et al. Among authors: mutchinick om. Am J Med Genet A. 2005 Apr 1;134A(1):49-57. doi: 10.1002/ajmg.a.30514. Am J Med Genet A. 2005. PMID: 15704121
123 results