Similar articles for PMID: 9598739

Year	Number of Results
1981	1
1993	1
1994	3
1995	2
1996	3
1997	1
1998	10
1999	4
2000	4
2001	8
2002	4
2003	3
2004	4
2005	5
2006	5
2007	2
2008	2
2011	4
2012	1
2013	1
2014	1
2017	3
2018	1
2019	2
2020	2
2021	2
2024	0

1

Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome.

Saraiva JM, Matoso E, Marques I. Saraiva JM, et al. J Med Genet. 1998 Apr;35(4):347-8. doi: 10.1136/jmg.35.4.347-a. J Med Genet. 1998. PMID: 9598739 Free PMC article. No abstract available.

2

Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?

Wulfsberg EA. Wulfsberg EA. Am J Med Genet. 1996 Aug 23;64(3):523-4. doi: 10.1002/ajmg.1320640303. Am J Med Genet. 1996. PMID: 8862634 No abstract available.

3

Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

Butler MG, Mowrey P. Butler MG, et al. J Med Genet. 1996 Aug;33(8):719-20. doi: 10.1136/jmg.33.8.719-a. J Med Genet. 1996. PMID: 8863172 Free PMC article. No abstract available.

4

[A phenotypic description of 26 patients with Ritscher-Schinzel syndrome (cranio-cerebello-cardiac dysplasia or 3C syndrome)].

Pira-Paredes SM, Montoya-Villada JH, Franco-Restrepo JL, Moncada-Velez M, Cornejo JW. Pira-Paredes SM, et al. Rev Neurol. 2017 Jun 1;64(11):481-488. Rev Neurol. 2017. PMID: 28555453 Free article. Spanish.

5

Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome.

Elder DA, Kaiser-Rogers K, Aylsworth AS, Calikoglu AS. Elder DA, et al. Am J Med Genet. 2001 Jun 1;101(1):17-9. doi: 10.1002/ajmg.1293. Am J Med Genet. 2001. PMID: 11343331

6

[Extra-cardiac phenotype associated with microdeletion 22q11].

Lacombe D. Lacombe D. Arch Pediatr. 2002 May;9 Suppl 2:100s-101s. doi: 10.1016/s0929-693x(01)00908-3. Arch Pediatr. 2002. PMID: 12108232 Review. French. No abstract available.

7

A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome.

Strenge S, Kujat A, Zelante L, Froster UG. Strenge S, et al. Am J Med Genet A. 2006 Dec 15;140(24):2838-9. doi: 10.1002/ajmg.a.31534. Am J Med Genet A. 2006. PMID: 17103454 No abstract available.

8

Myopathy in a patient with chromosome 22q11 deletion.

Mongini T, Doriguzzi C, Arduino C, Brusco A, Bortolotto S, Mutani R, Palmucci L. Mongini T, et al. Neuropediatrics. 2001 Apr;32(2):107-9. doi: 10.1055/s-2001-13877. Neuropediatrics. 2001. PMID: 11414642 No abstract available.

9

Cerebellar atrophy in a patient with velocardiofacial syndrome.

Lynch DR, McDonald-McGinn DM, Zackai EH, Emanuel BS, Driscoll DA, Whitaker LA, Fischbeck KH. Lynch DR, et al. J Med Genet. 1995 Jul;32(7):561-3. doi: 10.1136/jmg.32.7.561. J Med Genet. 1995. PMID: 7562973 Free PMC article.

10

Brown syndrome associated with velocardiofacial syndrome.

Chang S, Crowe CA, Traboulsi EI. Chang S, et al. J AAPOS. 2004 Jun;8(3):290-2. doi: 10.1016/j.jaapos.2004.01.012. J AAPOS. 2004. PMID: 15226737

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