PubMed (OMIM) for id: 340382

Year	Number of Results
1987	1
1989	1
1990	1
1991	3
1993	2
1994	1
2000	1
2024	0

1

Amor DJ, Woods CG. Amor DJ, et al. Clin Dysmorphol. 2000 Apr;9(2):115-8. doi: 10.1097/00019605-200009020-00008. Clin Dysmorphol. 2000. PMID: 10826623

2

Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.

Brown S, Gersen S, Anyane-Yeboa K, Warburton D. Brown S, et al. Am J Med Genet. 1993 Jan 1;45(1):52-9. doi: 10.1002/ajmg.1320450115. Am J Med Genet. 1993. PMID: 8418661 Review.

3

Pseudotrisomy 13 and autosomal recessive holoprosencephaly.

Seller MJ, Chitty LS, Dunbar H. Seller MJ, et al. J Med Genet. 1993 Nov;30(11):970-1. doi: 10.1136/jmg.30.11.970. J Med Genet. 1993. PMID: 8301659 Free PMC article.

4

Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.

Ramos-Arroyo MA, de Miguel C, Valiente A, Moreno-Laguna S. Ramos-Arroyo MA, et al. Am J Med Genet. 1994 Apr 1;50(2):177-9. doi: 10.1002/ajmg.1320500208. Am J Med Genet. 1994. PMID: 8010349

5

Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.

Young ID, Madders DJ. Young ID, et al. J Med Genet. 1987 Nov;24(11):714-5. doi: 10.1136/jmg.24.11.714. J Med Genet. 1987. PMID: 3430550 Free PMC article.

6

Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?

Hewitt BG, Seller MJ, Bennett CP, Maxwell DM. Hewitt BG, et al. Clin Genet. 1989 Aug;36(2):141-3. doi: 10.1111/j.1399-0004.1989.tb03177.x. Clin Genet. 1989. PMID: 2766571 No abstract available.

7

Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome.

Bachman H, Clark RD, Salahi W. Bachman H, et al. J Med Genet. 1990 Jan;27(1):50-2. doi: 10.1136/jmg.27.1.50. J Med Genet. 1990. PMID: 2407847 Free PMC article.

8

Pseudo-trisomy 13 syndrome.

Cohen MM Jr, Gorlin RJ. Cohen MM Jr, et al. Am J Med Genet. 1991 Jun 1;39(3):332-5; discussion 336-7. doi: 10.1002/ajmg.1320390316. Am J Med Genet. 1991. PMID: 1867286 Review.

9

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

10

Familial holoprosencephaly, heart defects, and polydactyly.

Hennekam RC, van Noort G, de la Fuente AA. Hennekam RC, et al. Am J Med Genet. 1991 Nov 1;41(2):258-62. doi: 10.1002/ajmg.1320410226. Am J Med Genet. 1991. PMID: 1785646 Review.

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