Thompson P - Search Results

1

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

Baker E, Hinton L, Callen DF, Altree M, Dobbie A, Eyre HJ, Sutherland GR, Thompson E, Thompson P, Woollatt E, Haan E. Baker E, et al. Among authors: thompson p, thompson e. Am J Med Genet. 2002 Feb 1;107(4):285-93. doi: 10.1002/ajmg.10159. Am J Med Genet. 2002. PMID: 11840484

2

Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene.

Sampson JR, Maheshwar MM, Aspinwall R, Thompson P, Cheadle JP, Ravine D, Roy S, Haan E, Bernstein J, Harris PC. Sampson JR, et al. Among authors: thompson p. Am J Hum Genet. 1997 Oct;61(4):843-51. doi: 10.1086/514888. Am J Hum Genet. 1997. PMID: 9382094 Free PMC article.

3

Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.

Archer HL, Gupta S, Enoch S, Thompson P, Rowbottom A, Chua I, Warren S, Johnson D, Ledbetter DH, Lese-Martin C, Williams P, Pilz DT. Archer HL, et al. Among authors: thompson p. Am J Med Genet A. 2005 Jul 1;136(1):38-44. doi: 10.1002/ajmg.a.30774. Am J Med Genet A. 2005. PMID: 15937949 Review.

4

A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay.

Upadhyaya M, Roberts SH, Maynard J, Sorour E, Thompson PW, Vaughan M, Wilkie AO, Hughes HE. Upadhyaya M, et al. Among authors: thompson pw. J Med Genet. 1996 Feb;33(2):148-52. doi: 10.1136/jmg.33.2.148. J Med Genet. 1996. PMID: 8929953 Free PMC article.

5

Four cases of acute leukemia with trisomy 4.

Thompson PW, Thompson EN, Whittaker JA. Thompson PW, et al. Among authors: thompson en. Cancer Genet Cytogenet. 1989 Dec;43(2):211-7. doi: 10.1016/0165-4608(89)90032-0. Cancer Genet Cytogenet. 1989. PMID: 2598165

6

Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome.

Keeling SL, Lee-Jones L, Thompson P. Keeling SL, et al. Among authors: thompson p. Am J Med Genet. 2001 Mar 1;99(2):94-8. doi: 10.1002/1096-8628(2000)9999:999<00::aid-ajmg1134>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11241465 Review.

7

Inheritance of CMT1A duplication from a mosaic father.

Sorour E, Thompson P, MacMillan J, Upadhyaya M. Sorour E, et al. Among authors: thompson p. J Med Genet. 1995 Jun;32(6):483-5. doi: 10.1136/jmg.32.6.483. J Med Genet. 1995. PMID: 7666403 Free PMC article.

8

15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.

Tatton-Brown K, Pilz DT, Orstavik KH, Patton M, Barber JC, Collinson MN, Maloney VK, Huang S, Crolla JA, Marks K, Ormerod E, Thompson P, Nawaz Z, Lese-Martin C, Tomkins S, Waits P, Rahman N, McEntagart M. Tatton-Brown K, et al. Among authors: thompson p. Am J Med Genet A. 2009 Feb;149A(2):147-54. doi: 10.1002/ajmg.a.32534. Am J Med Genet A. 2009. PMID: 19133692

9

Characterization of psu dic(6;5)(p21.3;q13) with reverse chromosome painting in a patient with secondary myelodysplastic syndrome following treatment for multiple myeloma.

Lee-Jones L, Ramsahoye B, Booth M, Thompson P, Whittaker J, Hoy T. Lee-Jones L, et al. Among authors: thompson p. Cancer Genet Cytogenet. 2004 Jan 1;148(1):49-54. doi: 10.1016/s0165-4608(03)00218-8. Cancer Genet Cytogenet. 2004. PMID: 14697641

10

Chromosome 2 interstitial deletion (del(2)(q14.1q21)) associated with connective tissue laxity and an attention deficit disorder.

Baker KL, Rees MI, Thompson PW, Howell RT, Cole TR, Houghes HE, Upadhyaya M, Ravine D. Baker KL, et al. Among authors: thompson pw. J Med Genet. 2001 Jul;38(7):493-6. doi: 10.1136/jmg.38.7.493. J Med Genet. 2001. PMID: 11476069 Free PMC article. Review. No abstract available.

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