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Issue Date
Title
Author(s)
2013
RAB40AL loss-of-function mutation does not cause X-linked intellectual disability
Kalscheuer, V.
;
Iqbal, Z.
;
Hu, H.
;
Haas, S.
;
Shaw, M.
;
Lebrun, N.
;
Seemanova, E.
;
Voesenek, K.
;
Hobson, L.
;
Ropers, H.H.
;
Townshend, S.
;
Raynaud, M.
;
van Bokhoven, H.
;
Riazuddin, S.
;
Chelly, J.
;
Gecz, J.
2014
UPF3B gene and nonsense-mediated mRNA decay in autism spectrum disorders
Laumonnier, F.
;
Nguyen, L.
;
Jolly, L.
;
Raynaud, M.
;
Gecz, J.
;
Patel, V.
;
Preedy, P.
;
Martin, C.
2012
Polycystic ovary syndrome: what do the new guidelines recommend?
Joham, A.
;
Teede, H.
;
Norman, R.
2014
Nonsense-mediated mRNA decay: Inter-individual variability and human disease
Nguyen, L.
;
Wilkinson, M.
;
Gecz, J.
2012
New mutations and sporadic intellectual disability
Gecz, J.
;
Haan, E.
2012
Does ovulation induction with follicle-stimulating hormone still have a future in polycystic ovary syndrome?
Norman, R.
Discover
Author
4
Gecz, J.
2
Nguyen, L.
2
Norman, R.
2
Raynaud, M.
1
Chelly, J.
1
Haan, E.
1
Haas, S.
1
Hobson, L.
1
Hu, H.
1
Iqbal, Z.
.
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Subject
2
920114 Reproductive System and Di...
2
Female
2
Humans
1
920106 Endocrine Organs and Disea...
1
920110 Inherited Diseases (incl. ...
1
Copy number variation
1
Exome
1
Expression quantitative trait loci
1
Fertilization in Vitro
1
Follicle Stimulating Hormone
.
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Date issued
2
2014
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2013
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2012