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                             34 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome Assink, Jacqueline J.M.
 1997
 61 4 p. 934-939
6 p.
 artikel
2 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 sepspaced 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 4 p. 991-993
3 p.
 artikel
3 A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p Brown, M.R.
 1997
 61 4 p. 924-927
4 p.
 artikel
4 Cell-Cycle Regulation of Mammalian DNA Double-Strand-Break Repair Hendrickson, Eric A.
 1997
 61 4 p. 795-800
6 p.
 artikel
5 Chorea-Acanthocytosis: Genetic Linkage to Chromosome 9q21 Rubio, Justin P.
 1997
 61 4 p. 899-908
10 p.
 artikel
6 Deletion of All CGG Repeats Plus Flanking Sequences in FMR1 Does Not Abolish Gene Expression Grønskov, Karen
 1997
 61 4 p. 961-967
7 p.
 artikel
7 Evidence for a Major Gene Controlling Susceptibility to Tegumentary Leishmaniasis in a Recently Exposed Bolivian Population Alcaïs, A.
 1997
 61 4 p. 968-979
12 p.
 artikel
8 Evidence for at Least Eight Fanconi Anemia Genes Joenje, Hans
 1997
 61 4 p. 940-944
5 p.
 artikel
9 Familial Glaucoma Iridogoniodysplasia Maps to a 6p25 Region Implicated in Primary Congenital Glaucoma and Iridogoniodysgenesis Anomaly Jordan, Tim
 1997
 61 4 p. 882-888
7 p.
 artikel
10 Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16 Szepetowski, Pierre
 1997
 61 4 p. 889-898
10 p.
 artikel
11 Fetal Cells in Maternal Circulation: Progress in Analysis of a Rare Event Goldberg, James D.
 1997
 61 4 p. 806-809
4 p.
 artikel
12 Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2 Horwitz, Marshall
 1997
 61 4 p. 873-881
9 p.
 artikel
13 Genome Scanning for Segments Shared Identical by Descent among Distant Relatives in Isolated Populations Durham, L. Kathryn
 1997
 61 4 p. 830-842
13 p.
 artikel
14 Hereditary Geniospasm: Linkage to Chromosome 9q13-q21 and Evidence for Genetic Heterogeneity Jarman, P.R.
 1997
 61 4 p. 928-933
6 p.
 artikel
15 Identification of Genetic Mutations in Japanese Patients with Fructose-1, 6-Bisphosphatase Deficiency Kikawa, Yoshiharu
 1997
 61 4 p. 852-861
10 p.
 artikel
16 Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23 Messina, David N.
 1997
 61 4 p. 909-917
9 p.
 artikel
17 Message Therapy: Gene Therapy That Targets mRNA Sequence and Stability Kozarsky, Karen F.
 1997
 61 4 p. 790-794
5 p.
 artikel
18 mtDNA Mutation Rates-No Need to Panic Macaulay, Vincent A.
 1997
 61 4 p. 983-986
4 p.
 artikel
19 Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins Adato, A.
 1997
 61 4 p. 813-821
9 p.
 artikel
20 Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome Bleyl, Steven B.
 1997
 61 4 p. 868-872
5 p.
 artikel
21 PCR Quantitation of Fetal Cells in Maternal Blood in Normal and Aneuploid Pregnancies * * Presented in part at the annual meeting of the Society for Pediatric Research, Washington, DC, May 7, 1996, and at the 46th meeting of the American Society of Human Genetics, San Francisco, October 31, 1996. Bianchi, Diana W.
 1997
 61 4 p. 822-829
8 p.
 artikel
22 Renal Cystic Disease in Tuberous Sclerosis: Role of the Polycystic Kidney Disease 1 Gene Sampson, Julian R.
 1997
 61 4 p. 843-851
9 p.
 artikel
23 Reply to Bandelt and Forster Weiss, Gunter
 1997
 61 4 p. 983-
1 p.
 artikel
24 Reply to Macauley et al. Howell, Neil
 1997
 61 4 p. 986-990
5 p.
 artikel
25 Reply to Macauley et al. HOWELL, NEIL
 1997
 61 4 p. 986-990
5 p.
 artikel
26 Risk Reversals in Predictive Testing for Huntington Disease Almqvist, Elisabeth
 1997
 61 4 p. 945-952
8 p.
 artikel
27 The Fate of Human Sperm-Derived mtDNA in Somatic Cells Manfredi, Giovanni
 1997
 61 4 p. 953-960
8 p.
 artikel
28 The Gene for Autosomal Dominant Craniometaphyseal Dysplasia Maps to Chromosome 5p and Is Distinct from the Growth Hormone-Receptor Gene Nürnberg, Peter
 1997
 61 4 p. 918-923
6 p.
 artikel
29 The Myth of Bumpy Hunter-Gatherer Mismatch Distributions Bandelt, Hans-Jürgen
 1997
 61 4 p. 980-983
4 p.
 artikel
30 The Promise and Reality of Cancer Gene Therapy Hall, Simon J.
 1997
 61 4 p. 785-789
5 p.
 artikel
31 The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies D'Adamo, Patrizia
 1997
 61 4 p. 862-867
6 p.
 artikel
32 This Month in the Journal Ashkenas, John
 1997
 61 4 p. i-ii
nvt p.
 artikel
33 Unconventional Myosins, the Basis for Deafness in Mouse and Man Hasson, Tama
 1997
 61 4 p. 801-805
5 p.
 artikel
34 What Is Significant in Whole-Genome Linkage Disequilibrium Studies? Kruglyak, Leonid
 1997
 61 4 p. 810-812
3 p.
 artikel
                             34 gevonden resultaten
 
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