Daniel A - Search Results

1

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

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

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.

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

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.

7

Molecular distinction between true centric fission and pericentric duplication-fission.

Perry J, Nouri S, La P, Daniel A, Wu Z, Purvis-Smith S, Northrop E, Choo KH, Slater HR. Perry J, et al. Among authors: daniel a. Hum Genet. 2005 Mar;116(4):300-10. doi: 10.1007/s00439-004-1209-4. Epub 2005 Jan 27. Hum Genet. 2005. PMID: 15712016

8

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

9

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases.

Bofinger MK, Opitz JM, Soukup SW, Ekblom LS, Phillips S, Daniel A, Greene EW. Bofinger MK, et al. Among authors: daniel a. Am J Med Genet. 1991 Jan;38(1):1-8. doi: 10.1002/ajmg.1320380102. Am J Med Genet. 1991. PMID: 2012119

10

Three different origins for apparent triploid/diploid mosaics.

Daniel A, Wu Z, Darmanian A, Collins F, Jackson J. Daniel A, et al. Prenat Diagn. 2003 Jul;23(7):529-34. doi: 10.1002/pd.634. Prenat Diagn. 2003. PMID: 12868076

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