Similar articles for PMID: 20104614

Year	Number of Results
1980	1
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2018	8
2021	2
2024	0

1

Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature.

Raam MS, Solomon BD, Shalev SA, Muenke M. Raam MS, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):176-82. doi: 10.1002/ajmg.c.30234. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104614 Free PMC article. Review.

2

Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature.

Keaton AA, Solomon BD, van Essen AJ, Pfleghaar KM, Slama MA, Martin JA, Muenke M. Keaton AA, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):170-5. doi: 10.1002/ajmg.c.30251. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104609 Free PMC article. Review.

3

Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosology.

Corona-Rivera JR, Trujillo-Ponce SA, Barrios-Prieto E, Quiles-Corona M, Miguel-Jimenez K, Aguirre-Guillen RL, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Genet Couns. 2013;24(1):45-55. Genet Couns. 2013. PMID: 23610864

4

Alobar holoprosencephaly associated with cebocephaly and craniosynostosis.

Lin CH, Tsai JD, Ho YJ, Lin WC. Lin CH, et al. Acta Neurol Taiwan. 2009 Jun;18(2):123-6. Acta Neurol Taiwan. 2009. PMID: 19673365

5

Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review.

Ionescu CA, Calin D, Navolan D, Matei A, Dimitriu M, Herghelegiu C, Ples L. Ionescu CA, et al. Medicine (Baltimore). 2018 Jul;97(29):e11521. doi: 10.1097/MD.0000000000011521. Medicine (Baltimore). 2018. PMID: 30024536 Free PMC article. Review.

6

Holoprosencephaly and primary craniosynostosis: the Genoa syndrome.

Camera G, Lituania M, Cohen MM Jr. Camera G, et al. Am J Med Genet. 1993 Dec 1;47(8):1161-5. doi: 10.1002/ajmg.1320470806. Am J Med Genet. 1993. PMID: 8291548

7

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.

8

Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil.

Richieri-Costa A, Ribeiro LA. Richieri-Costa A, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):149-57. doi: 10.1002/ajmg.c.30247. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104612 Review.

9

Genoa syndrome and central diabetes insipidus: a case report.

Hacıhamdioğlu B, Şıklar Z, Savaş Erdeve Ş, Berberoğlu M, Deda G, Tıraş ST, Fitöz S, Öcal G. Hacıhamdioğlu B, et al. J Clin Res Pediatr Endocrinol. 2010;2(2):89-91. doi: 10.4274/jcrpe.v2i2.89. Epub 2010 May 8. J Clin Res Pediatr Endocrinol. 2010. PMID: 21274346 Free PMC article.

10

Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.

Kauvar EF, Solomon BD, Curry CJ, van Essen AJ, Janssen N, Dutra A, Roessler E, Muenke M. Kauvar EF, et al. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):158-69. doi: 10.1002/ajmg.c.30235. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104613 Free PMC article. Review.

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