Similar articles for PMID: 20104610

Year	Number of Results
1982	1
1988	2
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2019	1
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2024	0

1

Holoprosencephaly due to numeric chromosome abnormalities.

Solomon BD, Rosenbaum KN, Meck JM, Muenke M. Solomon BD, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):146-8. doi: 10.1002/ajmg.c.30232. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104610 Free PMC article. Review.

2

Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?

Karmous-Benailly H, Tabet AC, Thaly A, Dupuy O, Huten Y, Luton D, Baumann C, Delezoide AL. Karmous-Benailly H, et al. Prenat Diagn. 2005 Mar;25(3):193-7. doi: 10.1002/pd.1102. Prenat Diagn. 2005. PMID: 15791668

3

Prenatal findings of holoprosencephaly.

Hayashi Y, Suzumori N, Sugiura T, Sugiura-Ogasawara M. Hayashi Y, et al. Congenit Anom (Kyoto). 2015 Aug;55(3):161-3. doi: 10.1111/cga.12103. Congenit Anom (Kyoto). 2015. PMID: 25620469

4

Syndromes associated with holoprosencephaly.

Kruszka P, Muenke M. Kruszka P, et al. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):229-237. doi: 10.1002/ajmg.c.31620. Epub 2018 May 17. Am J Med Genet C Semin Med Genet. 2018. PMID: 29770994 Free PMC article.

5

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).

Mercier S, Dubourg C, Belleguic M, Pasquier L, Loget P, Lucas J, Bendavid C, Odent S. Mercier S, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):191-6. doi: 10.1002/ajmg.c.30246. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104616 Review.

6

Holoprosencephaly: an antenatally-diagnosed case series and subject review.

Lim AS, Lim TH, Kee SK, Chia P, Raman S, Eu EL, Lim JY, Tien SL. Lim AS, et al. Ann Acad Med Singap. 2008 Jul;37(7):594-7. Ann Acad Med Singap. 2008. PMID: 18695774 Free article. Review.

7

Holoprosencephaly: An update on cytogenetic abnormalities.

Bendavid C, Dupé V, Rochard L, Gicquel I, Dubourg C, David V. Bendavid C, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):86-92. doi: 10.1002/ajmg.c.30250. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104602 Free article. Review.

8

Recognizing the clinical features of Trisomy 13 syndrome.

Rios A, Furdon SA, Adams D, Clark DA. Rios A, et al. Adv Neonatal Care. 2004 Dec;4(6):332-43. doi: 10.1016/j.adnc.2004.09.008. Adv Neonatal Care. 2004. PMID: 15609255

9

Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.

Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY. Chen CP, et al. Prenat Diagn. 2001 May;21(5):346-50. doi: 10.1002/pd.63. Prenat Diagn. 2001. PMID: 11360273 Review.

10

Holoprosencephaly.

Dubourg C, Bendavid C, Pasquier L, Henry C, Odent S, David V. Dubourg C, et al. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2-8. Orphanet J Rare Dis. 2007. PMID: 17274816 Free PMC article. Review.

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