| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
About the X-to-Y Gene Conversion Rate
|
Cruciani, Fulvio
|
|
2010
|
86 |
3 |
p. 495-497
3 p.
|
artikel
|
| 2 |
2009 ASHG Awards and Addresses
|
|
|
2010
|
86 |
3 |
p. 309-310
2 p.
|
artikel
|
| 3 |
A Weighted False Discovery Rate Control Procedure Reveals Alleles at FOXA2 that Influence Fasting Glucose Levels
|
Xing, Chao
|
|
2010
|
86 |
3 |
p. 440-446
7 p.
|
artikel
|
| 4 |
Brown-Vialetto-Van Laere Syndrome, a Ponto-Bulbar Palsy with Deafness, Is Caused by Mutations in C20orf54
|
Green, Peter
|
|
2010
|
86 |
3 |
p. 485-489
5 p.
|
artikel
|
| 5 |
Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E
|
Klopocki, Eva
|
|
2010
|
86 |
3 |
p. 434-439
6 p.
|
artikel
|
| 6 |
DNA Methylome of Familial Breast Cancer Identifies Distinct Profiles Defined by Mutation Status
|
Flanagan, James M.
|
|
2010
|
86 |
3 |
p. 420-433
14 p.
|
artikel
|
| 7 |
Evolutionary History of the ADRB2 Gene in Humans
|
Wilson, Richard H.
|
|
2010
|
86 |
3 |
p. 490-493
4 p.
|
artikel
|
| 8 |
Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations
|
Labuda, Damian
|
|
2010
|
86 |
3 |
p. 353-363
11 p.
|
artikel
|
| 9 |
Genetic Control of Individual Differences in Gene-Specific Methylation in Human Brain
|
Zhang, Dandan
|
|
2010
|
86 |
3 |
p. 411-419
9 p.
|
artikel
|
| 10 |
Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta
|
Christiansen, Helena E.
|
|
2010
|
86 |
3 |
p. 389-398
10 p.
|
artikel
|
| 11 |
Human ITCH E3 Ubiquitin Ligase Deficiency Causes Syndromic Multisystem Autoimmune Disease
|
Lohr, Naomi J.
|
|
2010
|
86 |
3 |
p. 447-453
7 p.
|
artikel
|
| 12 |
Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities
|
Ballif, Blake C.
|
|
2010
|
86 |
3 |
p. 454-461
8 p.
|
artikel
|
| 13 |
Identification of Uncommon Recurrent Potocki-Lupski Syndrome-Associated Duplications and the Distribution of Rearrangement Types and Mechanisms in PTLS
|
Zhang, Feng
|
|
2010
|
86 |
3 |
p. 462-470
9 p.
|
artikel
|
| 14 |
Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy
|
Kennerson, Marina L.
|
|
2010
|
86 |
3 |
p. 343-352
10 p.
|
artikel
|
| 15 |
Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)
|
Meyer, Esther
|
|
2010
|
86 |
3 |
p. 471-478
8 p.
|
artikel
|
| 16 |
Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss
|
Li, Yun
|
|
2010
|
86 |
3 |
p. 479-484
6 p.
|
artikel
|
| 17 |
No Evidence of Association of Heterozygous NTF4 Mutations in Patients with Primary Open-Angle Glaucoma
|
Liu, Yutao
|
|
2010
|
86 |
3 |
p. 498-499
2 p.
|
artikel
|
| 18 |
2009 Presidential Address: Beyond Darwin? Evolution, Coevolution, and the American Society of Human Genetics
|
McCabe, Edward R.B.
|
|
2010
|
86 |
3 |
p. 311-315
5 p.
|
artikel
|
| 19 |
2008 Presidential Address: Principia Genetica: Our Future Science
|
Chakravarti, Aravinda
|
|
2010
|
86 |
3 |
p. 302-308
7 p.
|
artikel
|
| 20 |
Regulation of Gene Expression by Small RNAs
|
Talebizadeh, Zohreh
|
|
2010
|
86 |
3 |
p. 328-330
3 p.
|
artikel
|
| 21 |
Response to Cruciani et al.
|
Rosser, Zoë H.
|
|
2010
|
86 |
3 |
p. 497-498
2 p.
|
artikel
|
| 22 |
Response to Liu et al.
|
Pasutto, Francesca
|
|
2010
|
86 |
3 |
p. 500-
1 p.
|
artikel
|
| 23 |
Response to Wilson et al.
|
Fumagalli, Matteo
|
|
2010
|
86 |
3 |
p. 493-495
3 p.
|
artikel
|
| 24 |
Systems Genetics Analysis of Gene-by-Environment Interactions in Human Cells
|
Romanoski, Casey E.
|
|
2010
|
86 |
3 |
p. 399-410
12 p.
|
artikel
|
| 25 |
Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79
|
Rehman, Atteeq Ur
|
|
2010
|
86 |
3 |
p. 378-388
11 p.
|
artikel
|
| 26 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2010
|
86 |
3 |
p. 299-301
3 p.
|
artikel
|
| 27 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2010
|
86 |
3 |
p. 297-298
2 p.
|
artikel
|
| 28 |
Using Principal Components of Genetic Variation for Robust and Powerful Detection of Gene-Gene Interactions in Case-Control and Case-Only Studies
|
Bhattacharjee, Samsiddhi
|
|
2010
|
86 |
3 |
p. 331-342
12 p.
|
artikel
|
| 29 |
2009 William Allan Award Address: Life in The Sandbox: Unfinished Business
|
Willard, Huntington F.
|
|
2010
|
86 |
3 |
p. 318-327
10 p.
|
artikel
|
| 30 |
2009 William Allan Award Introduction: Huntington F. Willard
|
Hassold, Terry
|
|
2010
|
86 |
3 |
p. 316-317
2 p.
|
artikel
|
| 31 |
Worldwide Population Analysis of the 4q and 10q Subtelomeres Identifies Only Four Discrete Interchromosomal Sequence Transfers in Human Evolution
|
Lemmers, Richard J.L.F.
|
|
2010
|
86 |
3 |
p. 364-377
14 p.
|
artikel
|
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