Saad A - Search Results

1

New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family.

Bouali N, Francou B, Bouligand J, Imanci D, Dimassi S, Tosca L, Zaouali M, Mougou S, Young J, Saad A, Guiochon-Mantel A. Bouali N, et al. Among authors: saad a. Fertil Steril. 2017 Oct;108(4):694-702. doi: 10.1016/j.fertnstert.2017.07.015. Epub 2017 Aug 30. Fertil Steril. 2017. PMID: 28863940 Free article.

2

Large duplication 4q25-q34 with mild clinical effect.

Elghezal H, Sendi HS, Monastiri K, Lapierre JM, Romdhane SI, Mougou S, Saad A. Elghezal H, et al. Among authors: saad a. Ann Genet. 2004 Oct-Dec;47(4):419-22. doi: 10.1016/j.anngen.2004.07.007. Ann Genet. 2004. PMID: 15581841

3

Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders.

Elghezal H, Hidar S, Braham R, Denguezli W, Ajina M, Saâd A. Elghezal H, et al. Among authors: saad a. Fertil Steril. 2006 Dec;86(6):1792-5. doi: 10.1016/j.fertnstert.2006.04.041. Epub 2006 Oct 23. Fertil Steril. 2006. PMID: 17056042 Free article.

4

Prevalence of chromosomal abnormalities in couples with recurrent miscarriage.

Elghezal H, Hidar S, Mougou S, Khairi H, Saâd A. Elghezal H, et al. Among authors: saad a. Fertil Steril. 2007 Sep;88(3):721-3. doi: 10.1016/j.fertnstert.2006.11.160. Epub 2007 Feb 23. Fertil Steril. 2007. PMID: 17320875 Free article.

5

Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.

Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A. Elghezal H, et al. Among authors: saad a. Eur J Med Genet. 2007 Nov-Dec;50(6):441-5. doi: 10.1016/j.ejmg.2007.07.002. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17851150

6

An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.

Gribaa M, Younes M, Bouyacoub Y, Korbaa W, Ben Charfeddine I, Touzi M, Adala L, Mamay O, Bergaoui N, Saad A. Gribaa M, et al. Among authors: saad a. J Bone Miner Metab. 2010;28(1):111-5. doi: 10.1007/s00774-009-0111-5. Epub 2009 Aug 5. J Bone Miner Metab. 2010. PMID: 19655082

7

Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype.

Ojeda D, Lakhal B, Fonseca DJ, Braham R, Landolsi H, Mateus HE, Restrepo CM, Elghezal H, Saâd A, Laissue P. Ojeda D, et al. Among authors: saad a. Fertil Steril. 2011 Jun 30;95(8):2658-60.e1. doi: 10.1016/j.fertnstert.2011.04.045. Epub 2011 May 14. Fertil Steril. 2011. PMID: 21575944 Free article.

8

Semen parameters and sperm DNA fragmentation as causes of recurrent pregnancy loss.

Brahem S, Mehdi M, Landolsi H, Mougou S, Elghezal H, Saad A. Brahem S, et al. Among authors: saad a. Urology. 2011 Oct;78(4):792-6. doi: 10.1016/j.urology.2011.05.049. Epub 2011 Aug 2. Urology. 2011. PMID: 21813165

9

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.

Ben Charfeddine I, Riepe FG, Kahloul N, Kulle AE, Adala L, Mamaï O, Amara A, Mili A, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: saad a. Gen Comp Endocrinol. 2012 Feb 1;175(3):514-8. doi: 10.1016/j.ygcen.2011.12.017. Epub 2011 Dec 22. Gen Comp Endocrinol. 2012. PMID: 22210247

10

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.

Ben-Abdallah-Bouhjar I, Hannachi H, Labalme A, Gmidène A, Mougou S, Soyah N, Gribaa M, Sanlaville D, Elghezal H, Saad A. Ben-Abdallah-Bouhjar I, et al. Among authors: saad a. Eur J Med Genet. 2012 Aug-Sep;55(8-9):461-5. doi: 10.1016/j.ejmg.2012.04.011. Epub 2012 Jun 7. Eur J Med Genet. 2012. PMID: 22683462

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

2,144 results

Search Page

Filters