2002-2003

1. Wang Z, Milunsky J, Yamin M, Maher T, Oates R, Milunsky A. Analysis by Mass Spectrometry of 100 cystic fibrosis gene mutations in 92 patients with congenital bilateral absence of the vas deferens. Human Reproduction 17:2066-2072;2002

2. Kirsch S, Weiss B, Kleiman S, Roberts K, Pryor J, Milunsky A, Ferlin A, Foresta C, Matthijs G, Simoni M, Rappold GA. Localization of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere. J Med Genet 39(7):507-513;2002.

3. Ma YX, Zhang SZ, Hou YP, Huang XL, Wu QQ, Sun Y.. Identification of a novel human zinc finger protein gene ZNF313. Biochem Journal 35(3):230-7;2003.

4. Moore LL, Singer, M., Rothman K, Milunsky A. Chromosomal Anomalies Among the Offspring of Women with Gestational Diabetes. Amer J Epidiol 155(8):719-724;2002.

5. Ma, Y, Zhang S, Xia Q, Zhang GE, Huang X-L, Huang M, Xiao C, Pan A, Sun Y, Lebo R Milunsky, A. Molecular characterization of the TCP11 gene which is the human homologue of the mouse gene encoding the receptor of fertilization promoting peptide. Mol. Human Reprod. 8(1):24-31;2002.

6. Moore LL, Bradlee ML, Singer MR, Rothman KJ, Milunsky A. Folate Intake and the Risk of Neural Tube Defects: An Estimation of Dose-Response. Epidemiology 14:200-205;2003.

7. Milunsky A. Lies, Damned Lies, and Medical Experts. The Abrogation of Responsibility by Specialty Organizations and a Call for Action. J Child Neur 2003;18:413.

8. Lebo RV, Wyandt HE, Warburton PE, Li S, Milunsky JM. An unstable dicentric Robertsonian translocation in a markedly discordant twin. Clin Genet 62(5):383-389;2002.

9. Milunsky JM, Maher TA, Metzenberg AB. Molecular, Biochemical, and Phenotypic Analysis of a Hemizygous Male With a Severe Atypical Phenotype for X-Linked Dominant Conradi-Hunermann-Happle Syndrome and a Mutation in EBP. Am J Med Genet 116(3):249-54;2003.

10. Milunsky JM, Capin DM. Cerebro-Oculo-Facial-Lymphatic Syndrome (COFL). Clin Genet 63:291-296;2003.

11. Stevenson VA, Ito M, Milunsky JM. Connexin 30 Deletion Analysis in Connexin 26 Heterozygotes. Genet Test 7:151-154; 2003.

12. Milunsky JM, Maher TA, Loose BA, Darras BT, Ito M. XL PCR for the Detection of Large Trinucleotide Expansions in juvenile Huntington’s disease. Clin Genet 64:70-73;2003.