nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Accurate Inference of Relationships in Sib-Pair Linkage Studies
|
Boehnke, Michael |
|
1997 |
61 |
2 |
p. 423-429 7 p. |
artikel |
2 |
Analysis of Genetic Linkage and Somatic Loss of Heterozygosity in Affected Pairs of First-Degree Relatives
|
Rohde, K. |
|
1997 |
61 |
2 |
p. 418-422 5 p. |
artikel |
3 |
Announcements 1 1 Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please mail announcements to The American Journal of Human Genetics, Department of Pathology, Box 357470, University of Washington, Seattle, WA 98195-7470, or fax them to (206) 685-9684. Submission must be received 3 full months before the month of issue in which publication is requested. They must be double spaced with a 1½-inch margin on all sides. The maximum length is 150 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member.
|
|
|
1997 |
61 |
2 |
p. 469-470 2 p. |
artikel |
4 |
A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus
|
Ferrero, Giovanni B. |
|
1997 |
61 |
2 |
p. 395-401 7 p. |
artikel |
5 |
Balanced Translocation 46, XY, t(2;15)(q37.2;q11.2) Associated with Atypical Prader-Willi Syndrome
|
Conroy, Jeffrey M. |
|
1997 |
61 |
2 |
p. 388-394 7 p. |
artikel |
6 |
Cancer Cytogenetics
|
Rowley, Janet D. |
|
1997 |
61 |
2 |
p. 468- 1 p. |
artikel |
7 |
Coding Mutations in p57 KIP2 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors
|
O'Keefe, Denise |
|
1997 |
61 |
2 |
p. 295-303 9 p. |
artikel |
8 |
Constitutional RB1-Gene Mutations in Patients with Isolated Unilateral Retinoblastoma
|
Lohmann, Dietmar R. |
|
1997 |
61 |
2 |
p. 282-294 13 p. |
artikel |
9 |
Embryonic Lethal Abnormal Visual RNA-Binding Proteins Involved in Growth, Differentiation, and Posttranscriptional Gene Expression
|
Antic, Dragana |
|
1997 |
61 |
2 |
p. 273-278 6 p. |
artikel |
10 |
Erratum
|
|
|
1997 |
61 |
2 |
p. 471- 1 p. |
artikel |
11 |
Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region
|
Arngrímsson, Reynir |
|
1997 |
61 |
2 |
p. 354-362 9 p. |
artikel |
12 |
Evidence for a Possible Asian Origin of YAP+ Y Chromosomes
|
ALTHEIDE, TASHA K. |
|
1997 |
61 |
2 |
p. 462-466 5 p. |
artikel |
13 |
Further Evidence Suggesting the Presence of a Locus, on Human Chromosome 5q31-q33, Influencing the Intensity of Infection with Schistosoma mansoni
|
Müller-Myhsok, Bertram |
|
1997 |
61 |
2 |
p. 452-454 3 p. |
artikel |
14 |
Genetic Counseling Is Directive? Look Again
|
KESSLER, SEYMOUR |
|
1997 |
61 |
2 |
p. 466-467 2 p. |
artikel |
15 |
Hemizygous Deletion of the Syntaxin 1A Gene in Individuals with Williams Syndrome
|
OSBORNE, LUCY R. |
|
1997 |
61 |
2 |
p. 449-452 4 p. |
artikel |
16 |
Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene Mutations
|
Wijnen, Juul |
|
1997 |
61 |
2 |
p. 329-335 7 p. |
artikel |
17 |
Identification and Analysis of Mutations in the Wilson Disease Gene (ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses
|
Shah, Anjali B. |
|
1997 |
61 |
2 |
p. 317-328 12 p. |
artikel |
18 |
Identification of a Duplication of Xq28 Associated with Bilateral Periventricular Nodular Heterotopia
|
Fink, James M. |
|
1997 |
61 |
2 |
p. 379-387 9 p. |
artikel |
19 |
Is There an Abnormal Phenotype Associated with Maternal Isodisomy for Chromosome 2 in the Presence of Two Isochromosomes?
|
SHAFFER, LISA G. |
|
1997 |
61 |
2 |
p. 461-462 2 p. |
artikel |
20 |
Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1
|
Ishikawa, K. |
|
1997 |
61 |
2 |
p. 336-346 11 p. |
artikel |
21 |
Linkage Analysis of 49 High-Risk Families Does Not Support a Common Familial Prostate Cancer—Susceptibility Gene at 1q24-25
|
McIndoe, Richard A. |
|
1997 |
61 |
2 |
p. 347-353 7 p. |
artikel |
22 |
Localization of a Gene for Autosomal Dominant Osteopetrosis (Albers-Schönberg Disease) to Chromosome 1p21
|
Van Hul, Wim |
|
1997 |
61 |
2 |
p. 363-369 7 p. |
artikel |
23 |
Localization of the Gene Causing Keratolytic Winter Erythema to Chromosome 8p22-p23, and Evidence for a Founder Effect in South African Afrikaans-Speakers
|
Starfield, Michelle |
|
1997 |
61 |
2 |
p. 370-378 9 p. |
artikel |
24 |
Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome
|
Lee, Maxwell P. |
|
1997 |
61 |
2 |
p. 304-309 6 p. |
artikel |
25 |
Multiple Sclerosis in Sardinia Is Associated and in Linkage Disequilibrium with HLA-DR3 and -DR4 Alleles
|
MARROSU, MARIA GIOVANNA |
|
1997 |
61 |
2 |
p. 454-457 4 p. |
artikel |
26 |
Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita
|
FERRARIS, ANNA MARIA |
|
1997 |
61 |
2 |
p. 458-461 4 p. |
artikel |
27 |
Predictive Testing for Retinoblastoma Comes of Age
|
Gallie, Brenda L. |
|
1997 |
61 |
2 |
p. 279-281 3 p. |
artikel |
28 |
Spectrum of Mutations in the Batten Disease Gene, CLN3
|
Munroe, Patricia B. |
|
1997 |
61 |
2 |
p. 310-316 7 p. |
artikel |
29 |
Tests for Linkage and Association in Nuclear Families
|
Martin, E.R. |
|
1997 |
61 |
2 |
p. 439-448 10 p. |
artikel |
30 |
The Apo(a) Gene is the Major Determinant of Variation in Plasma Lp(a) Levels in African Americans
|
Mooser, Vincent |
|
1997 |
61 |
2 |
p. 402-417 16 p. |
artikel |
31 |
The Final Stage of Gene Expression: Chaperones and the Regulation of Protein Fate
|
Ashkenas, John |
|
1997 |
61 |
2 |
p. 267-272 6 p. |
artikel |
32 |
The Regulation of Splice-Site Selection, and Its Role in Human Disease
|
Cooper, Thomas A. |
|
1997 |
61 |
2 |
p. 259-266 8 p. |
artikel |
33 |
This Month in the Journal
|
Ashkenas, John |
|
1997 |
61 |
2 |
p. i-ii nvt p. |
artikel |
34 |
True and False Positive Peaks in Genomewide Scans: Applications of Length-Biased Sampling to Linkage Mapping
|
Terwilliger, Joseph D. |
|
1997 |
61 |
2 |
p. 430-438 9 p. |
artikel |