E-LIB Suche - Ergebnisse für: Flinter, F.

1

P–788 Health outcomes at birth, 12 and 24 months of 747 chi..:

Trevisan, L ; Forzano, F ; Khalaf, Y...
Human Reproduction. 36 (2021) Supplement_1 - p. , 2021

Link: https://doi.org/10.1093/..

2

Collagen type IV-related nephropathies in Portugal: pathoge..:

Nabais Sá, M.J. ; Storey, H. ; Flinter, F....
Clinical Genetics. 88 (2014) 5 - p. 456-461 , 2014

Link: https://doi.org/10.1111/..

3

858 Genetic profile of cystinuria in a UK population – the ..:

Wong, K.A. ; Pardy, C. ; Mein, R....
European Urology Supplements. 11 (2012) 1 - p. e858-e858a , 2012

Link: https://doi.org/10.1016/..

4

Meiotic segregation of Robertsonian translocations ascertai..:

Bint, S. M. ; Mackie Ogilvie, C. ; Flinter, F. A...
Human Reproduction. 26 (2011) 6 - p. 1575-1584 , 2011

Link: https://doi.org/10.1093/..

5

Autosomal dominant inheritance of non-syndromic renal hypop..:

Kerecuk, L. ; Sajoo, A. ; McGregor, L....
Nephrology Dialysis Transplantation. 22 (2006) 1 - p. 259-263 , 2006

Link: https://doi.org/10.1093/..

6

Three hundred and thirty cycles of preimplantation genetic ..:

Grace, J ; El‐Toukhy, T ; Scriven, P...
BJOG: An International Journal of Obstetrics & Gynaecology. 113 (2006) 12 - p. 1393-1401 , 2006

Link: https://doi.org/10.1111/..

7

O▪59 Paediatric outcome from birth to 2 years after PGD:

Lashwood, A ; Kanabar, D ; Braude, P.
Reproductive BioMedicine Online. 10 (2005) - p. 19 , 2005

Link: https://doi.org/10.1016/..

8

Terminal deletion of chromosome 5p in a patient with phenot..:

Stathopulu, E. ; Ogilvie, C. Mackie ; Flinter, F.A.
American Journal of Medical Genetics Part A. 119A (2003) 3 - p. 363-366 , 2003

Link: https://doi.org/10.1002/..

9

Multiple endocrine neoplasia type 1 (MEN1) germline mutatio..:

Pannett, A. A. J. ; Kennedy, A. M. ; Turner, J. J. O....
Clinical Endocrinology. 58 (2003) 5 - p. 639-646 , 2003

Link: https://doi.org/10.1046/..

10

A novel G472R mutation in a Turkish family with X-linked Al..:

Topaloglu, R. ; Plant, K. E. ; Flinter, F.
Pediatric Nephrology. 14 (2000) 6 - p. 480-481 , 2000

Link: https://doi.org/10.1007/..

11

Chromosome 11q13 and atopic asthma:

Adra, C N ; Mao, X‐Q ; Kawada, H...
Clinical Genetics. 55 (1999) 6 - p. 431-437 , 1999

Link: https://doi.org/10.1034/..

12

Why are mutations in COL4A5 not detectable in all patients ..:

Flinter, F. ; Plant, K.
Nephrology Dialysis Transplantation. 13 (1998) 6 - p. 1348-1351 , 1998

Link: https://doi.org/10.1093/..

13

Evidence of a locus for orofacial clefting on human chromos..:

F.Davles, A. ; J.Stephens, R. ; G.OIavesen, M....
Human Molecular Genetics. 4 (1995) 1 - p. 121-128 , 1995

Link: https://doi.org/10.1093/..

14

Becker muscular dystrophy presenting with complete heart bl..:

Quinlivan, R. ; Ball, J. ; Dunckley, M....
Journal of Neurology. 242 (1995) 6 - p. 398-400 , 1995

Link: https://doi.org/10.1007/..

15

A clinical and molecular genetic study of dentatorubropalli..:

Warner, T. T. ; Williams, L. D. ; Walker, R. W. H....
Annals of Neurology. 37 (1995) 4 - p. 452-459 , 1995

Link: https://doi.org/10.1002/..