Fisher AM - Search Results

1

Centromeric inactivation in a dicentric human Y;21 translocation chromosome.

Fisher AM, Al-Gazali L, Pramathan T, Quaife R, Cockwell AE, Barber JC, Earnshaw WC, Axelman J, Migeon BR, Tyler-Smith C. Fisher AM, et al. Chromosoma. 1997 Sep;106(4):199-206. doi: 10.1007/s004120050240. Chromosoma. 1997. PMID: 9254721

2

Small terminal deletions of the long arm of chromosome 2: two new cases.

Fisher AM, Ellis KH, Browne CE, Barber JC, Barker M, Kennedy CR, Foley H, Patton MA. Fisher AM, et al. Am J Med Genet. 1994 Dec 1;53(4):366-9. doi: 10.1002/ajmg.1320530412. Am J Med Genet. 1994. PMID: 7532357

3

Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels.

Fisher AM, Barber JC, Crolla JA, James RS, Lestas AN, Jennings I, Dennis NR. Fisher AM, et al. Am J Med Genet. 1993 Aug 1;47(1):100-5. doi: 10.1002/ajmg.1320470121. Am J Med Genet. 1993. PMID: 8368238 Review.

4

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.

Fisher AM, Thomas NS, Cockwell A, Stecko O, Kerr B, Temple IK, Clayton P. Fisher AM, et al. Hum Genet. 2002 Sep;111(3):290-6. doi: 10.1007/s00439-002-0787-2. Epub 2002 Jul 20. Hum Genet. 2002. PMID: 12215843

5

Three patients with ring (X) chromosomes and a severe phenotype.

Dennis NR, Collins AL, Crolla JA, Cockwell AE, Fisher AM, Jacobs PA. Dennis NR, et al. Among authors: fisher am. J Med Genet. 1993 Jun;30(6):482-6. doi: 10.1136/jmg.30.6.482. J Med Genet. 1993. PMID: 8326492 Free PMC article.

6

Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samples.

Fisher AM, Cockwell AE, Moore KJ, Gregson NM, Campbell PL, Campbell CM, Herbert A, Barber JC, Crolla JA. Fisher AM, et al. Prenat Diagn. 1996 Jul;16(7):615-21. doi: 10.1002/(SICI)1097-0223(199607)16:7<615::AID-PD920>3.0.CO;2-9. Prenat Diagn. 1996. PMID: 8843470

7

Incidence of circulating cells positive for GpIb and GpIIIa in infants with Down's syndrome.

Fisher AM, Cockwell AE, Jacobs PA, Parry HF. Fisher AM, et al. Eur J Haematol. 1994 Jul;53(1):46-8. doi: 10.1111/j.1600-0609.1994.tb00178.x. Eur J Haematol. 1994. PMID: 8062897

8

RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.

Power MM, James RS, Barber JC, Fisher AM, Wood PJ, Leatherdale BA, Flanagan DE, Hatchwell E. Power MM, et al. Among authors: fisher am. J Med Genet. 1997 Apr;34(4):287-90. doi: 10.1136/jmg.34.4.287. J Med Genet. 1997. PMID: 9138150 Free PMC article.

9

Inv(10)(p11.2q21.2), a variant chromosome.

Collinson MN, Fisher AM, Walker J, Currie J, Williams L, Roberts P. Collinson MN, et al. Among authors: fisher am. Hum Genet. 1997 Dec;101(2):175-80. doi: 10.1007/s004390050609. Hum Genet. 1997. PMID: 9402964 Review.

10

Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports.

Law CJ, Fisher AM, Temple IK. Law CJ, et al. Among authors: fisher am. J Med Genet. 1998 Aug;35(8):685-9. doi: 10.1136/jmg.35.8.685. J Med Genet. 1998. PMID: 9719381 Free PMC article. Review.

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