Crocker M - Search Results

1

Congenital disseminated neurofibromatosis type 1: a clinical and molecular case report.

Stewart H, Bowker C, Edees S, Smalley S, Crocker M, Mechan D, Forrester N, Spurlock G, Upadhyaya M. Stewart H, et al. Among authors: crocker m. Am J Med Genet A. 2008 Jun 1;146A(11):1444-52. doi: 10.1002/ajmg.a.32305. Am J Med Genet A. 2008. PMID: 18438896

2

Cryptic mosaicism for monosomy 20 identified in renal tract cells.

Stefanou EG, Crocker M, Boon A, Stewart H. Stefanou EG, et al. Among authors: crocker m. Clin Genet. 2006 Sep;70(3):228-32. doi: 10.1111/j.1399-0004.2006.00652.x. Clin Genet. 2006. PMID: 16922725

3

An unbalanced autosomal translocation (7;9) associated with feminization.

Crocker M, Coghill SB, Cortinho R. Crocker M, et al. Clin Genet. 1988 Jul;34(1):70-3. doi: 10.1111/j.1399-0004.1988.tb02618.x. Clin Genet. 1988. PMID: 3409542

4

Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes.

Tyler-Smith C, Oakey RJ, Larin Z, Fisher RB, Crocker M, Affara NA, Ferguson-Smith MA, Muenke M, Zuffardi O, Jobling MA. Tyler-Smith C, et al. Among authors: crocker m. Nat Genet. 1993 Dec;5(4):368-75. doi: 10.1038/ng1293-368. Nat Genet. 1993. PMID: 8298645

5

A sibship with Roberts/SC phocomelia syndrome.

Holmes-Siedle M, Seres-Santamaria A, Crocker M, Hall JG, Crouchman M. Holmes-Siedle M, et al. Among authors: crocker m. Am J Med Genet. 1990 Sep;37(1):18-22. doi: 10.1002/ajmg.1320370106. Am J Med Genet. 1990. PMID: 2240038

6

A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.

Babbs C, Heller R, Everman DB, Crocker M, Twigg SR, Schwartz CE, Giele H, Wilkie AO. Babbs C, et al. Among authors: crocker m. Hum Genet. 2007 Sep;122(2):191-9. doi: 10.1007/s00439-007-0390-7. Epub 2007 Jun 14. Hum Genet. 2007. PMID: 17569090

7

Maternal 3;13 chromosome insertion, with severe pre-eclampsia.

Boyd PA, Maher EJ, Lindenbaum RH, Hoogwerf AM, Redman C, Crocker M. Boyd PA, et al. Among authors: crocker m. Clin Genet. 1995 Jan;47(1):17-21. doi: 10.1111/j.1399-0004.1995.tb03915.x. Clin Genet. 1995. PMID: 7774038

8

Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated moderate bilateral ventriculomegaly.

Stefanou EG, Hanna G, Foakes A, Crocker M, Fitchett M. Stefanou EG, et al. Among authors: crocker m. Prenat Diagn. 2002 Jan;22(1):64-6. doi: 10.1002/pd.243. Prenat Diagn. 2002. PMID: 11810654

9

A chromosome 21-derived minute marker in a mosaic trisomy 21 background: implications for risk assessments in marker chromosome cases.

Stefanou EG, Crocker M. Stefanou EG, et al. Among authors: crocker m. Am J Med Genet A. 2004 Jun 1;127A(2):191-3. doi: 10.1002/ajmg.a.20682. Am J Med Genet A. 2004. PMID: 15108209

10

An unusual case of X-15 translocation: evidence for the presence of an 'activator' region on Xpter of man.

Crocker M, Jonasson J, Patel C. Crocker M, et al. Clin Genet. 1985 Dec;28(6):556-60. doi: 10.1111/j.1399-0004.1985.tb00426.x. Clin Genet. 1985. PMID: 3865752

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