Ellis PM - Search Results

1

Symmetrical upper limb peromelia and lower limb phocomelia associated with a de novo apparently balanced reciprocal translocation: 46,XX,t(2; 12)(p25.1;q24.1).

Murray RS, Keeling JW, Ellis PM, FitzPatrick DR. Murray RS, et al. Among authors: ellis pm. Clin Dysmorphol. 2002 Apr;11(2):87-90. doi: 10.1097/00019605-200204000-00002. Clin Dysmorphol. 2002. PMID: 12002154

2

Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y-chromosome-specific in situ hybridisation.

Ellis PM, West JD, West KM, Murray RS, Coyle MC. Ellis PM, et al. Mol Reprod Dev. 1990 Jan;25(1):37-41. doi: 10.1002/mrd.1080250107. Mol Reprod Dev. 1990. PMID: 2393582

3

Clinical follow-up of high mid-trimester maternal serum intact human chorionic gonadotrophin concentrations in singleton pregnancies.

Blundell G, Ashby JP, Martin C, Shearing CH, Langdale-Brown B, Keeling J, Ellis PM, Shade M, Chambers SE, Wenham PR. Blundell G, et al. Among authors: ellis pm. Prenat Diagn. 1999 Mar;19(3):219-23. doi: 10.1002/(sici)1097-0223(199903)19:3<219::aid-pd512>3.0.co;2-k. Prenat Diagn. 1999. PMID: 10210119

4

ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome.

Brown DC, Grace E, Sumner AT, Edmunds AT, Ellis PM. Brown DC, et al. Among authors: ellis pm. Hum Genet. 1995 Oct;96(4):411-6. doi: 10.1007/BF00191798. Hum Genet. 1995. PMID: 7557962 Review.

5

A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves.

Sumner AT, Mitchell AR, Ellis PM. Sumner AT, et al. Among authors: ellis pm. J Med Genet. 1998 Oct;35(10):833-5. doi: 10.1136/jmg.35.10.833. J Med Genet. 1998. PMID: 9783707 Free PMC article.

6

An aetiological study of isochromosome-X Turner's syndrome.

Carothers AD, De Mey R, Daker M, Boyd E, Connor M, Ellis PM, Stevenson D. Carothers AD, et al. Among authors: ellis pm. Clin Genet. 1989 Jul;36(1):53-8. doi: 10.1111/j.1399-0004.1989.tb03366.x. Clin Genet. 1989. PMID: 2766563

7

Cytogenetic abnormalities in childhood acute lymphoblastic leukemia.

Micallef-Eynaud PD, Eden OB, Grace E, Ellis PM. Micallef-Eynaud PD, et al. Among authors: ellis pm. Pediatr Hematol Oncol. 1993 Jan-Mar;10(1):25-30. doi: 10.3109/08880019309016524. Pediatr Hematol Oncol. 1993. PMID: 8443048

8

'Typus edinburgensis' explained.

Laing IA, Lyall EG, Hendry LM, Ellis PM. Laing IA, et al. Among authors: ellis pm. Pediatrics. 1991 Jul;88(1):151-4. Pediatrics. 1991. PMID: 2057251 No abstract available.

9

Acute lymphoblastic leukemia and Klinefelter's syndrome.

Shaw MP, Eden OB, Grace E, Ellis PM. Shaw MP, et al. Among authors: ellis pm. Pediatr Hematol Oncol. 1992 Jan-Mar;9(1):81-5. doi: 10.3109/08880019209006400. Pediatr Hematol Oncol. 1992. PMID: 1558779

10

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings.

Carothers AD, Boyd E, Lowther G, Ellis PM, Couzin DA, Faed MJ, Robb A. Carothers AD, et al. Among authors: ellis pm. Genet Epidemiol. 1999;16(2):179-90. doi: 10.1002/(SICI)1098-2272(1999)16:2<179::AID-GEPI5>3.0.CO;2-7. Genet Epidemiol. 1999. PMID: 10030400

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