1. Wyandt HE, Shim SH, Huang XL, Mark HFL, Milunsky JM. Duplication of 11p14.3-p15.1 in a Mentally Retarded Proband and his mother detected by G-Banding and Confirmed by High-Resolution CGH and BAC FISH. Exp Mol Pathol 80: 262-266; 2006.

2. Milunsky JM, Zhao G, Maher TA, Colby R, Everman DB. LADD syndrome is caused by FGF10 mutations. Clin Genet 69: 349-354; 2006.

3. Flynn M, Milunsky JM. Autosomal Dominant Syndrome Resembling Coffin-Siris Syndrome. Am J Med Genet 140A: 1326-1330; 2006.

4. Vaglio A, Gonzalo G, Bernal M, Sanguinetti C, Mechoso B, Quadrelli A, Tucci P, Milunsky JM, Huang XL, Pagano S, Quadrelli R. Prenatal and Postnatal characterization of a de novo Xq22.1 terminal deletion. Genet Test 10: 272-276; 2006.

5. Milunsky J and Milunsky A. Genetic Counseling in Prenatal and Perinatal Medicine. In Clinical Obstetrics. E.A. Reece and J.C.Hobbins (Editors), 2nd Ed. Lippincott-Raven, Philadelphia.

6. Wyandt, H, Tonk VJ, Huang X-L, Evans AT, Milunsky JM, Milunsky A. Correlation of Abnormal Rapid FISH and Chromosome Results from Amniocytes for Prenatal Diagnosis. FETAL DIAG THER 21(2):235-240;2006.

7. Hantash FM, Milunsky A, Wang Z, Anderson B, Sun W, Anguiano A, Strom CM. A Large Deletion in the CFTR Gene in a CBAVD patient. GENET MED 2006:8(2):93-95.

8. Sun W, Anderson B, Redman J, Milunsky A, Buller A, McGinniss M, Quan F, Anguiano A, Huang S, Hantash F, Strom S. The CFTR 5T Variant has a Low Penetrance in Females that is Partially Attributable to its Haplotype. Genet Med 2006:8(6):339-345.

9. Mechoso B, Vaglio A, Quadrelli A, Mark HFL, Huang X-L, Milunsky A, Quadrelli R. A De Novo Complex Chromosome Rearrangement Involving Chromosomes 2,3,5,9 and 11 Detected Prenatally and Studied Postnatally by Conventional Cytogenetics and Molecular Analyses. FETAL DIAGN THER 2007;22(4):249-53.

10. Vaglio A, Milunsky A, Huang, X-L, Quardrelli A, Mechoso B, Quadrelli R. Partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12. Eur J Med Genet. 2007 May-Jun;50(3):224-32.

11. Vaglio A, Milunsky A, Huang XL, Quadrelli A, Mechoso B, Quardrelli R. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: Clinical, cytogenetic and molecular observations. Eur J Med Genet. 2007 May-Jun;50(3):224-32.