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Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c. 109C>T (p. R37X).
Published in:
Clinical Genetics, 2015, v. 87, n. 5, p. 461, doi. 10.1111/cge.12420
By:
- Basehore, M.J.;
- Michaelson‐Cohen, R.;
- Levy‐Lahad, E.;
- Sismani, C.;
- Bird, L.M.;
- Friez, M.J.;
- Walsh, T.;
- Abidi, F.;
- Holloway, L.;
- Skinner, C.;
- McGee, S.;
- Alexandrou, A.;
- Syrrou, M.;
- Patsalis, P.C.;
- Raymond, G.;
- Wang, T.;
- Schwartz, C.E.;
- King, M.‐C.;
- Stevenson, R.E.
Publication type:
Article
Effect of Percoll gradient and swim-up preparation on the chromomycin A[sub3] staining of normal and abnormal semen samples.
Published in:
Andrologia, 1998, v. 30, n. 2, p. 101
By:
- Georgiou, I.;
- Syrrou, M.;
- Stefanidis, K.;
- Konstantelli, M.;
- Lolis, D.
Publication type:
Article
Promoter hypermethylation of the MEG3 (DLK1/MEG3) imprinted gene in multiple myeloma.
Published in:
2008
By:
- Benetatos L;
- Dasoula A;
- Hatzimichael E;
- Georgiou I;
- Syrrou M;
- Bourantas KL
Publication type:
Journal Article
Lack of Association of Birth Size with Polymorphisms of Two Imprinted Genes, IGF2R and GRB10.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2004, v. 17, n. 9, p. 1215, doi. 10.1515/jpem.2004.17.9.1215
By:
- Kukuvitis, A.;
- Georgiou, I.;
- Syrrou, M.;
- Andronikou, S.;
- Dickerman, Z.;
- Islam, A.;
- McCann, J.;
- Polychronakos, C.
Publication type:
Article
Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization.
Published in:
1997
By:
- Georgiou, I;
- Konstantelli, M;
- Syrrou, M;
- Messinis, I E;
- Lolis, D E
Publication type:
journal article
Skewed X-Chromosome Inactivation in Greek Women with Idiopathic Recurrent Miscarriage.
Published in:
Fetal Diagnosis & Therapy, 2008, v. 23, n. 3, p. 198, doi. 10.1159/000116741
By:
- Dasoula, A.;
- Kalantaridou, S.;
- Sotiriadis, A.;
- Pavlou, M.;
- Georgiou, I.;
- Paraskevaidis, E.;
- Makrigiannakis, A.;
- Syrrou, M.
Publication type:
Article

Found: 6

Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c. 109C>T (p. R37X).

Effect of Percoll gradient and swim-up preparation on the chromomycin A[sub3] staining of normal and abnormal semen samples.

Promoter hypermethylation of the MEG3 (DLK1/MEG3) imprinted gene in multiple myeloma.

Lack of Association of Birth Size with Polymorphisms of Two Imprinted Genes, IGF2R and GRB10.

Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization.

Skewed X-Chromosome Inactivation in Greek Women with Idiopathic Recurrent Miscarriage.