E-LIB Suche - Ergebnisse für: Hart, P Suzanne

1

An International Summit in Human Genetics and Genomics: Emp..:

Kaur, Manjit ; Hadley, Donald W. ; Muenke, Maximilian.
Molecular Genetics & Genomic Medicine. 7 (2019) 1 - p. , 2019

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

2

Cover:

Kaur, Manjit ; Hadley, Donald W. ; Muenke, Maximilian.
Molecular Genetics & Genomic Medicine. 7 (2019) 1 - p. , 2019

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

3

Medical genetics and genomic medicine in the United States ..:

Ferreira, Carlos R. ; Regier, Debra S. ; Hadley, Donald W...
Molecular Genetics & Genomic Medicine. 5 (2017) 4 - p. 307-316 , 2017

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

4

Invited commentary: The need for human genetics and genomic..:

Hart, P. Suzanne ; Hart, Thomas C.
Molecular Genetics & Genomic Medicine. 4 (2016) 2 - p. 123-125 , 2016

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

5

Foreword to volume 3, issue 6:

Hart, P. Suzanne ; Muenke, Maximilian
Molecular Genetics & Genomic Medicine. 3 (2015) 6 - p. 481-482 , 2015

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

6

Craniodentofacial Manifestations in a Rare Syndrome: Orofac..:

Ozdemir-Karatas, Meltem ; Ozdemir-Ozenen, Didem ; Hart, P. Suzanne.
Case Reports in Dentistry. 2014 (2014) - p. 1-5 , 2014

Link: https://doi.org/10.1155/..

7

Contributors:

, In: Principles and Practice of Clinical Research,

Albert, Paul S. ; Bartlett, Olivia T. ; Bates, Angela... - p. ix-xi , 2012

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

8

Penetrance of PD in Glucocerebrosidase Gene Mutation Carrie..:

Sidransky, Ellen ; Hart, P. Suzanne
Neurology. 79 (2012) 1 - p. 106-107 , 2012

Link: https://doi.org/10.1212/..

9

Identification of 2 novel ANTXR2 mutations in patients with..:

Denadai, Rafael ; Raposo‐Amaral, Cassio E. ; Bertola, Débora...
American Journal of Medical Genetics Part A. 158A (2012) 4 - p. 732-742 , 2012

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

10

Harnessing Information Using Genomic Platforms:

, In: Principles and Practice of Clinical Research,

Hart, P. Suzanne ; Markello, Thomas C. ; Gahl, William A. - p. 727-744 , 2012

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

11

Chediak–Higashi syndrome with early developmental delay res..:

Manoli, Irini ; Golas, Gretchen ; Westbroek, Wendy...
American Journal of Medical Genetics Part A. 152A (2010) 6 - p. 1474-1483 , 2010

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

12

Childhood course of renal insufficiency in a family with a ..:

Schäffer, Péter ; Gombos, Éva ; Meichelbeck, Krisztina...
Pediatric Nephrology. 25 (2010) 7 - p. 1355-1360 , 2010

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

13

Exclusion of candidate genes in seven Turkish families with..:

Becerik, Sema ; Cogulu, Dilsah ; Emingil, Gülnur...
American Journal of Medical Genetics Part A. 149A (2009) 7 - p. 1392-1398 , 2009

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

14

A 4 bp deletion mutation in DLX3 enhances osteoblastic diff..:

Choi, Sun Jin ; Song, In Sun ; Ryu, Ok Hee...
Bone. 42 (2008) 1 - p. 162-171 , 2008

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

15

Exclusion of known gene for enamel development in two Brazi..:

Santos, Maria CLG ; Hart, P Suzanne ; Ramaswami, Mukundhan...
Head & Face Medicine. 3 (2007) 1 - p. , 2007

Link: https://doi.org/10.1186/..