Roland B - Search Results

1

An interstitial deletion of the long arm of chromosome 13.

Roland B, Lowry RB, Robertson AS, Cox DM. Roland B, et al. Clin Genet. 1989 Apr;35(4):276-81. doi: 10.1111/j.1399-0004.1989.tb02943.x. Clin Genet. 1989. PMID: 2469548 Review.

2

A familial interstitial deletion of the long arm of chromosome 21.

Roland B, Cox DM, Hoar DI, Fowlow SB, Robertson AS. Roland B, et al. Clin Genet. 1990 Jun;37(6):423-8. doi: 10.1111/j.1399-0004.1990.tb03525.x. Clin Genet. 1990. PMID: 2383928

3

Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q14 to 6q16.

Roland B, Lowry RB, Cox DM, Ferreira P, Lin CC. Roland B, et al. Clin Genet. 1993 Mar;43(3):117-21. doi: 10.1111/j.1399-0004.1993.tb04434.x. Clin Genet. 1993. PMID: 8500257

4

9qh+ variant band in two families.

Roland B, Chernos JE, Cox DM. Roland B, et al. Am J Med Genet. 1992 Jan 1;42(1):137-8. doi: 10.1002/ajmg.1320420128. Am J Med Genet. 1992. PMID: 1308354 No abstract available.

5

Sex chromosome mosaicism not detected at amniocentesis.

Roland B, Cox DM, Rudd NL. Roland B, et al. Prenat Diagn. 1990 May;10(5):333-6. doi: 10.1002/pd.1970100509. Prenat Diagn. 1990. PMID: 2143821

6

Basic cytogenetics for office practice.

Roland B, Cox DM. Roland B, et al. Can Fam Physician. 1988 Apr;34:875-9. Can Fam Physician. 1988. PMID: 21253093 Free PMC article.

7

Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.

Xu J, Chernos J, Roland B. Xu J, et al. Among authors: roland b. Am J Med Genet. 1997 Dec 19;73(3):327-9. Am J Med Genet. 1997. PMID: 9415693

8

Trisomy 21 and isodicentric chromosome 21 in Kostmann syndrome following treatment with G-CSF.

Roland B, Woodman RC, Jorgenson K, Pinto A. Roland B, et al. Cancer Genet Cytogenet. 2001 Apr 1;126(1):78-80. doi: 10.1016/s0165-4608(00)00393-9. Cancer Genet Cytogenet. 2001. PMID: 11343785

9

Evidence of chromosome 9 origin of the euchromatic variant band within 9qh.

Hoo JJ, Szego K, Wong P, Roland B. Hoo JJ, et al. Among authors: roland b. Clin Genet. 1993 Jun;43(6):309-11. doi: 10.1111/j.1399-0004.1993.tb03824.x. Clin Genet. 1993. PMID: 8370151

10

Ring chromosome 7 with amplification of 7q sequences in a pediatric case of hepatosplenic T-cell lymphoma.

Shetty S, Mansoor A, Roland B. Shetty S, et al. Among authors: roland b. Cancer Genet Cytogenet. 2006 Jun;167(2):161-3. doi: 10.1016/j.cancergencyto.2005.12.003. Cancer Genet Cytogenet. 2006. PMID: 16737917

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