PubMed (cited) for id: 125520

Year	Number of Results
1967	1
1969	1
1972	2
1974	1
1976	1
1979	2
1980	1
1986	1
1993	1
1994	2
1995	1
1996	1
1997	1
1998	2
2003	1
2004	2
2024	0

1

EYA1 mutation in a newborn female presenting with cardiofacial syndrome.

Shimasaki N, Watanabe K, Hara M, Kosaki K. Shimasaki N, et al. Pediatr Cardiol. 2004 Jul-Aug;25(4):411-3. doi: 10.1007/s00246-003-0271-3. Pediatr Cardiol. 2004. PMID: 15493068

2

A review of 35 cases of asymmetric crying facies.

Caksen H, Odabaş D, Tuncer O, Kirimi E, Tombul T, Ikbal M, Ataş B, Ari Yuca S. Caksen H, et al. Genet Couns. 2004;15(2):159-65. Genet Couns. 2004. PMID: 15287415

3

Vasomotor instability in neonates with chromosome 22q11 deletion syndrome.

Shashi V, Berry MN, Hines MH. Shashi V, et al. Am J Med Genet A. 2003 Sep 1;121A(3):231-4. doi: 10.1002/ajmg.a.20219. Am J Med Genet A. 2003. PMID: 12923863

4

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.

Matsuoka R, Kimura M, Scambler PJ, Morrow BE, Imamura S, Minoshima S, Shimizu N, Yamagishi H, Joh-o K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K. Matsuoka R, et al. Hum Genet. 1998 Jul;103(1):70-80. doi: 10.1007/s004390050786. Hum Genet. 1998. PMID: 9737780

5

Monozygotic twins concordant for Cayler syndrome.

Rauch A, Hofbeck M, Bähring S, Leipold G, Trautmann U, Singer H, Pfeiffer RA. Rauch A, et al. Am J Med Genet. 1998 Jan 6;75(1):113-7. Am J Med Genet. 1998. PMID: 9450869

6

Frequency of associated anomalies in congenital hypoplasia of depressor anguli oris muscle: a study of 50 patients.

Lin DS, Huang FY, Lin SP, Chen MR, Kao HA, Hung HY, Hsu CH. Lin DS, et al. Am J Med Genet. 1997 Aug 8;71(2):215-8. Am J Med Genet. 1997. PMID: 9217225

7

Monozygotic twins with 22q11 deletion and discordant phenotypes.

Fryer A. Fryer A. J Med Genet. 1996 Feb;33(2):173. doi: 10.1136/jmg.33.2.173. J Med Genet. 1996. PMID: 8929959 Free PMC article. No abstract available.

8

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Goodship J, Cross I, Scambler P, Burn J. Goodship J, et al. J Med Genet. 1995 Sep;32(9):746-8. doi: 10.1136/jmg.32.9.746. J Med Genet. 1995. PMID: 8544199 Free PMC article.

9

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Burn J, et al. J Med Genet. 1993 Oct;30(10):822-4. doi: 10.1136/jmg.30.10.822. J Med Genet. 1993. PMID: 8230157 Free PMC article.

10

Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype.

Giannotti A, Digilio MC, Marino B, Mingarelli R, Dallapiccola B. Giannotti A, et al. Am J Med Genet. 1994 Nov 15;53(3):303-4. doi: 10.1002/ajmg.1320530320. Am J Med Genet. 1994. PMID: 7856669 No abstract available.

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