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

Year Number of Results
1989 1
1990 1
1991 4
1992 1
1993 2
1996 3
1997 2
1999 1
2000 4
2001 7
2002 2
2003 6
2004 1
2005 4
2006 5
2007 3
2008 3
2009 4
2010 6
2011 5
2012 3
2013 4
2015 3
2016 2
2017 3
2019 1
2020 2
2021 1
2022 1
2024 1
2025 3

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83 results

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Page 1
Branchiooculofacial Syndrome.
Haldeman-Englert CR, Lin AE, Milunsky JM. Haldeman-Englert CR, et al. Among authors: milunsky jm. 2011 May 31 [updated 2025 Aug 14]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2011 May 31 [updated 2025 Aug 14]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 21634087 Free Books & Documents. Review.
Hypermobile Ehlers-Danlos Syndrome: Cerebrovascular, Autonomic and Neuropathic Features.
Novak P, Systrom DM, Marciano SP, Witte A, Warren A, Felsenstein D, Giannetti MP, Hamilton MJ, Nicoloro-SantaBarbara J, Castells M, Farhad K, Pilgrim DM, Mullally WJ, Fishman MC, Milunsky JM, Milunsky A, Krier J. Novak P, et al. Among authors: milunsky jm. Am J Med Open. 2025 Jul 18;14:100111. doi: 10.1016/j.ajmo.2025.100111. eCollection 2025 Dec. Am J Med Open. 2025. PMID: 40843452 Free PMC article.
Waardenburg Syndrome Type I.
Milunsky JM. Milunsky JM. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301703 Free Books & Documents. Review.
ARID1B-related disorder in 87 adults: Natural history and self-sustainability.
van der Sluijs PJ, Gösgens M, Dingemans AJM, Striano P, Riva A, Mignot C, Faudet A, Vasileiou G, Walther M, Schrier Vergano SA, Alders M, Alkuraya FS, Alorainy I, Alsaif HS, Anderlid B, Bache I, van Beek I, Blanluet M, van Bon BW, Brunet T, Brunner H, Carriero ML, Charles P, Chatron N, Coccia E, Dubourg C, Earl RK, Eichler EE, Faivre L, Foulds N, Graziano C, Guerrot AM, Hashem MO, Heide S, Heron D, Hickey SE, Hopman SMJ, Kattentidt-Mouravieva A, Kerkhof J, Klein Wassink-Ruiter JS, Kurtz-Nelson EC, Kušíková K, Kvarnung M, Lecoquierre F, Leszinski GS, Loberti L, Magoulas PL, Mari F, Maystadt I, Merla G, Milunsky JM, Moortgat S, Nicolas G, Leary MO', Odent S, Ozmore JR, Parbhoo K, Pfundt R, Piccione M, Pinto AM, Popp B, Putoux A, Rehm HL, Reis A, Renieri A, Rosenfeld JA, Rossi M, Salzano E, Saugier-Veber P, Seri M, Severi G, Sonmez FM, Strobl-Wildemann G, Stuurman KE, Uctepe E, Van Esch H, Vitetta G, de Vries BBA, Wahl D, Wang T, Zacher P, Heitink KR, Ropers FG, Steenbeek D, Rybak T, Santen GWE. van der Sluijs PJ, et al. Among authors: milunsky jm. Genet Med Open. 2024 Jul 23;2:101873. doi: 10.1016/j.gimo.2024.101873. eCollection 2024. Genet Med Open. 2024. PMID: 39669611 Free PMC article.
Cerebro-oculo-facial-lymphatic syndrome.
Milunsky JM, Capin DM. Milunsky JM, et al. Clin Genet. 2003 Apr;63(4):291-6. doi: 10.1034/j.1399-0004.2003.00052.x. Clin Genet. 2003. PMID: 12702162
LADD syndrome is caused by FGF10 mutations.
Milunsky JM, Zhao G, Maher TA, Colby R, Everman DB. Milunsky JM, et al. Clin Genet. 2006 Apr;69(4):349-54. doi: 10.1111/j.1399-0004.2006.00597.x. Clin Genet. 2006. PMID: 16630169
Mutation analysis in Rett syndrome.
Milunsky JM, Lebo RV, Ikuta T, Maher TA, Haverty CE, Milunsky A. Milunsky JM, et al. Genet Test. 2001 Winter;5(4):321-5. doi: 10.1089/109065701753617462. Genet Test. 2001. PMID: 11960578
Familial supernumerary chromosome and malignancy.
Milunsky JM, Wyandt HE, Milunsky A. Milunsky JM, et al. Cancer Genet Cytogenet. 1996 Jul 15;89(2):170-2. doi: 10.1016/0165-4608(96)00069-6. Cancer Genet Cytogenet. 1996. PMID: 8697427 Free article.
83 results