Golbus MS - Search Results

1

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.

Lebo RV, Chance PF, Dyck PJ, Redila-Flores MT, Lynch ED, Golbus MS, Bird TD, King MC, Anderson LA, Hall J, et al. Lebo RV, et al. Among authors: golbus ms. Hum Genet. 1991 Nov;88(1):1-12. doi: 10.1007/BF00204921. Hum Genet. 1991. PMID: 1683643

2

Prenatal diagnosis of alpha-thalassemia by polymerase chain reaction and dual restriction enzyme analysis.

Lebo RV, Saiki RK, Swanson K, Montano MA, Erlich HA, Golbus MS. Lebo RV, et al. Among authors: golbus ms. Hum Genet. 1990 Aug;85(3):293-9. doi: 10.1007/BF00206749. Hum Genet. 1990. PMID: 1975558

3

Somatic mosaicism at the Duchenne locus.

Lebo RV, Olney RK, Golbus MS. Lebo RV, et al. Among authors: golbus ms. Am J Med Genet. 1990 Oct;37(2):187-90. doi: 10.1002/ajmg.1320370206. Am J Med Genet. 1990. PMID: 1978985

4

The polymorphic Fc gamma receptor II gene maps to human chromosome 1q.

Grundy HO, Peltz G, Moore KW, Golbus MS, Jackson LG, Lebo RV. Grundy HO, et al. Among authors: golbus ms. Immunogenetics. 1989;29(5):331-9. doi: 10.1007/BF00352843. Immunogenetics. 1989. PMID: 2565886

5

Prenatal diagnosis with repetitive in situ hybridization probes.

Lebo RV, Flandermeyer RR, Diukman R, Lynch ED, Lepercq JA, Golbus MS. Lebo RV, et al. Among authors: golbus ms. Am J Med Genet. 1992 Jul 15;43(5):848-54. doi: 10.1002/ajmg.1320430519. Am J Med Genet. 1992. PMID: 1642274

6

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.

Lebo RV, Lynch ED, Bird TD, Golbus MS, Barker DF, O'Connell P, Chance PF. Lebo RV, et al. Among authors: golbus ms. Am J Hum Genet. 1992 Jan;50(1):42-55. Am J Hum Genet. 1992. PMID: 1729894 Free PMC article.

7

Rapid determination of fetal sex by deoxyribonucleic acid amplification of Y chromosome-specific sequences.

Pinckert TL, Lebo RV, Golbus MS. Pinckert TL, et al. Among authors: golbus ms. Am J Obstet Gynecol. 1989 Sep;161(3):693-8. doi: 10.1016/0002-9378(89)90382-7. Am J Obstet Gynecol. 1989. PMID: 2782353

8

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes.

Katayama S, Montano M, Slotnick RN, Lebo RV, Golbus MS. Katayama S, et al. Among authors: golbus ms. Am J Obstet Gynecol. 1988 Mar;158(3 Pt 1):548-55. doi: 10.1016/0002-9378(88)90023-3. Am J Obstet Gynecol. 1988. PMID: 2894769

9

Prenatal diagnosis of hemophilia involving grandpaternal mosaicism.

Lebo RV, Koerper MA, Kim JH, Chueh J, Golbus MS. Lebo RV, et al. Among authors: golbus ms. Am J Med Genet. 1993 Sep 1;47(3):401-4. doi: 10.1002/ajmg.1320470321. Am J Med Genet. 1993. PMID: 7907841

10

Prenatal diagnosis of unusual hemoglobinopathies.

Kim JH, Lebo RV, Cai SP, Su X, Chung JH, Mentzer WC, Golbus MS. Kim JH, et al. Among authors: golbus ms. Am J Med Genet. 1994 Mar 1;50(1):15-20. doi: 10.1002/ajmg.1320500104. Am J Med Genet. 1994. PMID: 8160747

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