Daniel A - Search Results

1

Identification of marker chromosomes in thirteen patients using FISH probing.

Daniel A, Malafiej P, Preece K, Chia N, Nelson J, Smith M. Daniel A, et al. Am J Med Genet. 1994 Oct 15;53(1):8-18. doi: 10.1002/ajmg.1320530103. Am J Med Genet. 1994. PMID: 7802042 Review.

2

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.

Daniel A, Baker E, Chia N, Haan E, Malafiej P, Hinton L, Clarke N, Adès L, Darmanian A, Callen D. Daniel A, et al. Am J Med Genet A. 2003 Feb 15;117A(1):57-64. doi: 10.1002/ajmg.a.10048. Am J Med Genet A. 2003. PMID: 12548741 Review.

3

A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15.

Daniel A, Malafiej P. Daniel A, et al. Am J Med Genet A. 2003 Mar 15;117A(3):212-22. doi: 10.1002/ajmg.a.10100. Am J Med Genet A. 2003. PMID: 12599184 Review.

4

Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.

Li S, Malafiej P, Levy B, Mahmood R, Field M, Hughes T, Lockhart LH, Wu Z, Huang M, Hirschhorn K, Velagaleti GV, Daniel A, Warburton PE. Li S, et al. Among authors: daniel a. Am J Med Genet. 2002 Jul 1;110(3):258-67. doi: 10.1002/ajmg.10454. Am J Med Genet. 2002. PMID: 12116235

5

A study of early amniocentesis for prenatal cytogenetic diagnosis.

Daniel A, Ng A, Kuah KB, Reiha S, Malafiej P. Daniel A, et al. Prenat Diagn. 1998 Jan;18(1):21-8. Prenat Diagn. 1998. PMID: 9483636

6

An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection.

Mahjoubi F, Peters GB, Malafiej P, Shalhoub C, Turner A, Daniel A, Hill RJ. Mahjoubi F, et al. Among authors: daniel a. Cytogenet Genome Res. 2005;109(4):485-90. doi: 10.1159/000084207. Cytogenet Genome Res. 2005. PMID: 15905642

7

Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism.

Daniel A, Wu Z, Darmanian A, Malafiej P, Tembe V, Peters G, Kennedy C, Adès L. Daniel A, et al. Prenat Diagn. 2004 Jul;24(7):524-36. doi: 10.1002/pd.936. Prenat Diagn. 2004. PMID: 15300743 Review.

8

Karyotype, phenotype and parental origin in 19 cases of triploidy.

Daniel A, Wu Z, Bennetts B, Slater H, Osborn R, Jackson J, Pupko V, Nelson J, Watson G, Cooke-Yarborough C, Loo C. Daniel A, et al. Prenat Diagn. 2001 Dec;21(12):1034-48. doi: 10.1002/pd.164. Prenat Diagn. 2001. PMID: 11746161

9

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

Daniel A, Hook EB, Wulf G. Daniel A, et al. Am J Med Genet. 1989 May;33(1):14-53. doi: 10.1002/ajmg.1320330105. Am J Med Genet. 1989. PMID: 2750783

Pooled carriers (either sex) of 2:2 segregating rcp of mode 1 had a risk of 20-25% whereas female Robertsonian (rob) translocation (D;21) carriers and pericentric inversion (pii) carriers of pii with small distal segments had a risk of 10-15%. Pooled 2:2 segregating …

Pooled carriers (either sex) of 2:2 segregating rcp of mode 1 had a risk of 20-25% whereas female Robertsonian (rob) translocation (D …

10

An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies.

Daniel A, Darmanian A, Peters G, Goodwin L, Hort JR. Daniel A, et al. Am J Med Genet A. 2007 Oct 15;143A(20):2452-9. doi: 10.1002/ajmg.a.31960. Am J Med Genet A. 2007. PMID: 17853472

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