Temtamy SA - Search Results

1

Haplotypes and mutations of the PAH locus in Egyptian families with PKU.

Effat L, Kuzmin A, Kasem N, Meguid NA, Kotb S, Eisensmith RC, Temtamy SA, Rushdi S, Woo S, el-Awady M. Effat L, et al. Among authors: temtamy sa. Eur J Hum Genet. 1999 Feb-Mar;7(2):259-62. doi: 10.1038/sj.ejhg.5200270. Eur J Hum Genet. 1999. PMID: 10196714

2

GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.

Meguid NA, Afifi HH, Ramzy MI, Hindawy A, Temtamy SA. Meguid NA, et al. Among authors: temtamy sa. Clin Genet. 1997 Aug;52(2):110-5. doi: 10.1111/j.1399-0004.1997.tb02527.x. Clin Genet. 1997. PMID: 9298746

3

Hypogenitalism in the acrocallosal syndrome.

Temtamy SA, Meguid NA. Temtamy SA, et al. Am J Med Genet. 1989 Mar;32(3):301-5. doi: 10.1002/ajmg.1320320304. Am J Med Genet. 1989. PMID: 2658583 Review.

4

Molecular analysis of androgen resistance syndromes in Egyptian patients.

Essawi M, Gad YZ, el-Rouby O, Temtamy SA, Sabour YA, el-Awady MK. Essawi M, et al. Among authors: temtamy sa. Dis Markers. 1997 Apr;13(2):99-105. Dis Markers. 1997. PMID: 9160185

5

Lenz microphthalmia syndrome: three additional cases with rare associated anomalies.

Temtamy SA, Ismail SI, Meguid NA. Temtamy SA, et al. Genet Couns. 2000;11(2):147-52. Genet Couns. 2000. PMID: 10893665

6

Orodental, ear and eye anomalies in Egyptian Brachmann de Lange syndrome cases.

Temtamy SA, Aboul-Ezz EH, Simbawy AH, Mouenis AL, Meguid NA, El-Sawi M. Temtamy SA, et al. J Egypt Public Health Assoc. 1994;69(3-4):163-84. J Egypt Public Health Assoc. 1994. PMID: 17265636

7

COFS syndrome with familial 1;16 translocation.

Temtamy SA, Meguid NA, Mahmoud A, Afifi HH, Gerzawy A, Zaki MS. Temtamy SA, et al. Clin Genet. 1996 Oct;50(4):240-3. doi: 10.1111/j.1399-0004.1996.tb02635.x. Clin Genet. 1996. PMID: 9001808

8

An epidemiological/genetic study of mental subnormality in Assiut Governorate, Egypt.

Temtamy SA, Kandil MR, Demerdash AM, Hassan WA, Meguid NA, Afifi HH. Temtamy SA, et al. Clin Genet. 1994 Nov;46(5):347-51. doi: 10.1111/j.1399-0004.1994.tb04176.x. Clin Genet. 1994. PMID: 7889643

9

Heterozygous expression of Lesch-Nyhan syndrome clinical and ultrastructural studies.

Meguid NA, Aboul-Ezz EH, Seif E, Temtamy SA. Meguid NA, et al. Among authors: temtamy sa. J Egypt Public Health Assoc. 1990;65(5-6):585-600. J Egypt Public Health Assoc. 1990. PMID: 2134093

10

Direct molecular analysis of the fragile X syndrome in a sample of Egyptian and German patients using non-radioactive PCR and Southern blot followed by chemiluminescent detection.

el-Aleem AA, Böhm I, Temtamy S, el-Awady M, Awadalla M, Schmidtke J, Stuhrmann M. el-Aleem AA, et al. Hum Genet. 1995 Nov;96(5):577-84. doi: 10.1007/BF00197414. Hum Genet. 1995. PMID: 8530006

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