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                             34 gevonden resultaten
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
                             34 gevonden resultaten
 
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