Genel M - Search Results

1

Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.

Lichter JB, Wu JS, Genel M, Flynn SD, Pakstis AJ, Kidd JR, Kidd KK. Lichter JB, et al. Among authors: genel m. J Clin Endocrinol Metab. 1992 Feb;74(2):368-73. doi: 10.1210/jcem.74.2.1346145. J Clin Endocrinol Metab. 1992. PMID: 1346145

2

The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.

Wu JS, Carson NL, Myers S, Pakstis AJ, Kidd JR, Castiglione CM, Anderson L, Hoyle LS, Genel M, Verdy M, et al. Wu JS, et al. Among authors: genel m. Am J Hum Genet. 1990 Mar;46(3):624-30. Am J Hum Genet. 1990. PMID: 1968709 Free PMC article.

3

Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy.

Gill JR, Reyes-Múgica M, Iyengar S, Kidd KK, Touloukian RJ, Smith C, Keller MS, Genel M. Gill JR, et al. Among authors: genel m. J Pediatr. 1996 Sep;129(3):459-64. doi: 10.1016/s0022-3476(96)70084-7. J Pediatr. 1996. PMID: 8804341 Free article.

4

Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in children.

Heptulla RA, Schwartz RP, Bale AE, Flynn S, Genel M. Heptulla RA, et al. Among authors: genel m. J Pediatr. 1999 Sep;135(3):327-31. doi: 10.1016/s0022-3476(99)70129-0. J Pediatr. 1999. PMID: 10484798 Free article.

5

Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded.

Kidd KK, Kidd JR, Castiglione CM, Genel M, Darby J, Cavalli-Sforza LL, Gusella JF. Kidd KK, et al. Among authors: genel m. Hum Hered. 1986;36(4):243-9. doi: 10.1159/000153634. Hum Hered. 1986. PMID: 2875939

6

One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.

Pakstis AJ, Kidd JR, Castiglione CM, Pletcher BA, Murphy PD, Farrer LA, Genel M, Kidd KK. Pakstis AJ, et al. Among authors: genel m. Henry Ford Hosp Med J. 1987;35(2-3):164-7. Henry Ford Hosp Med J. 1987. PMID: 2891651 Free article. No abstract available.

7

Linkage analyses of multiple endocrine neoplasia, type 2 (MEN-2) with 23 classical genetic polymorphisms.

Kruger SD, Gertner JM, Sparkes RS, Haedt LE, Crist M, Sparkes MC, Genel M, Kidd KK. Kruger SD, et al. Among authors: genel m. Hum Hered. 1986;36(1):6-11. doi: 10.1159/000153592. Hum Hered. 1986. PMID: 2868987

8

Provocative testing for occult medullary carcinoma of the thyroid: findings in seven children with multiple endocrine neoplasia type IIa.

Graham SM, Genel M, Touloukian RJ, Barwick KW, Gertner JM, Torony C. Graham SM, et al. Among authors: genel m. J Pediatr Surg. 1987 Jun;22(6):501-3. doi: 10.1016/s0022-3468(87)80205-1. J Pediatr Surg. 1987. PMID: 2886576

9

Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.

Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI. Pang S, et al. Among authors: genel m. J Clin Endocrinol Metab. 1980 Mar;50(3):586-9. doi: 10.1210/jcem-50-3-586. J Clin Endocrinol Metab. 1980. PMID: 6244328

10

Suppression of the growth hormone (GH) response to clonidine and GH-releasing hormone by exogenous GH.

Nakamoto JM, Gertner JM, Press CM, Hintz RL, Rosenfeld RG, Genel M. Nakamoto JM, et al. Among authors: genel m. J Clin Endocrinol Metab. 1986 May;62(5):822-6. doi: 10.1210/jcem-62-5-822. J Clin Endocrinol Metab. 1986. PMID: 3082919

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

135 results

Search Page

Filters