Eng CM - Search Results

1

The lifetime risks of breast cancer in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations.

Satagopan JM, Offit K, Foulkes W, Robson ME, Wacholder S, Eng CM, Karp SE, Begg CB. Satagopan JM, et al. Among authors: eng cm. Cancer Epidemiol Biomarkers Prev. 2001 May;10(5):467-73. Cancer Epidemiol Biomarkers Prev. 2001. PMID: 11352856

2

Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patients.

Fodor FH, Weston A, Bleiweiss IJ, McCurdy LD, Walsh MM, Tartter PI, Brower ST, Eng CM. Fodor FH, et al. Among authors: eng cm. Am J Hum Genet. 1998 Jul;63(1):45-51. doi: 10.1086/301903. Am J Hum Genet. 1998. PMID: 9634504 Free PMC article.

3

Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases.

Eng CM, Desnick RJ. Eng CM, et al. Adv Genet. 2001;44:275-96. doi: 10.1016/s0065-2660(01)44086-7. Adv Genet. 2001. PMID: 11596990 Review.

4

Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.

Li L, Eng C, Desnick RJ, German J, Ellis NA. Li L, et al. Mol Genet Metab. 1998 Aug;64(4):286-90. doi: 10.1006/mgme.1998.2733. Mol Genet Metab. 1998. PMID: 9758720

5

Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews.

Dong J, Katz DR, Eng CM, Kornreich R, Desnick RJ. Dong J, et al. Among authors: eng cm. Mol Genet Metab. 2001 Jun;73(2):160-3. doi: 10.1006/mgme.2001.3182. Mol Genet Metab. 2001. PMID: 11386851

6

Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.

Sherman JB, Raben N, Nicastri C, Argov Z, Nakajima H, Adams EM, Eng CM, Cowan TM, Plotz PH. Sherman JB, et al. Among authors: eng cm. Am J Hum Genet. 1994 Aug;55(2):305-13. Am J Hum Genet. 1994. PMID: 8037209 Free PMC article.

7

HLA-DQA1 and polymarker allele frequencies in two New York City Jewish populations.

Medintz I, Levine L, McCurdy L, Chiriboga L, Kingston C, Crim D, Desnick RJ, Eng CM, Kobilinsky L. Medintz I, et al. Among authors: eng cm. J Forensic Sci. 1997 Sep;42(5):919-22. J Forensic Sci. 1997. PMID: 9304843

8

Molecular prenatal diagnosis of glycogen storage disease type Ia.

Qu Y, Abdenur JE, Eng CM, Desnick RJ. Qu Y, et al. Among authors: eng cm. Prenat Diagn. 1996 Apr;16(4):333-6. doi: 10.1002/(SICI)1097-0223(199604)16:4<333::AID-PD861>3.0.CO;2-G. Prenat Diagn. 1996. PMID: 8734807

9

Fabry disease: twenty-two novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations in severely and mildly affected hemizygotes and heterozygotes.

Ashton-Prolla P, Tong B, Shabbeer J, Astrin KH, Eng CM, Desnick RJ. Ashton-Prolla P, et al. Among authors: eng cm. J Investig Med. 2000 Jul;48(4):227-35. J Investig Med. 2000. PMID: 10916280

10

Pulmonary involvement in Fabry disease.

Brown LK, Miller A, Bhuptani A, Sloane MF, Zimmerman MI, Schilero G, Eng CM, Desnick RJ. Brown LK, et al. Among authors: eng cm. Am J Respir Crit Care Med. 1997 Mar;155(3):1004-10. doi: 10.1164/ajrccm.155.3.9116979. Am J Respir Crit Care Med. 1997. PMID: 9116979

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