Prevalence of the Fragile X Syndrome in African-Americans (English)
- New search for: Crawford, D. C.
- New search for: Meadows, K. L.
- New search for: Newman, J. L.
- New search for: Taft, L. F.
- New search for: Scott, E.
- New search for: Leslie, M.
- New search for: Shubek, L.
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- New search for: Yeargin-Allsopp, M.
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- New search for: Taft, L. F.
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In:
AMERICAN JOURNAL OF MEDICAL GENETICS
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110
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226-233
;
2002
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ISSN:
- Article (Journal) / Print
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Title:Prevalence of the Fragile X Syndrome in African-Americans
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Contributors:Crawford, D. C. ( author ) / Meadows, K. L. ( author ) / Newman, J. L. ( author ) / Taft, L. F. ( author ) / Scott, E. ( author ) / Leslie, M. ( author ) / Shubek, L. ( author ) / Holmgreen, P. ( author ) / Yeargin-Allsopp, M. ( author ) / Boyle, C. ( author )
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Published in:AMERICAN JOURNAL OF MEDICAL GENETICS ; 110 ; 226-233
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Publisher:
- New search for: JOHN WILEY & SONS LTD
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Publication date:2002-01-01
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Size:8 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616.042
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616.042 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 110
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 3
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Genetic Counseling for Sex Chromosome AbnormalitiesLinden, M. G. / Bender, B. G. / Robinson, A. et al. | 2002
- 11
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Fifty-One Prenatally Diagnosed Children and Adolescents With Sex Chromosome AbnormalitiesLinden, M. G. / Bender, B. G. et al. | 2002
- 19
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Significant Impact of the Highly Informative (CA)~n Repeat Polymorphism of the APOA-II Gene on the Plasma APOA-II Concentrations and HDL Subfractions: The ECTIM StudyBrousseau, T. / Dupuy-Gorce, A.-M. / Evans, A. / Arveiler, D. / Ruidavets, J.-B. / Haas, B. / Cambou, J.-P. / Luc, G. / Ducimetiere, P. / Amouyel, P. et al. | 2002
- 25
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C7 Complement Deficiency in an Israeli Arab VillageBehar, D. / Schlesinger, M. / Halle, D. / Ben-Ami, H. / Edoute, Y. / Shahar, E. / Kasis, I. / Shihab, S. / Elstein, D. / Zimran, A. et al. | 2002
- 30
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Lack of Association of the Two Polymorphisms in Alpha-2 Macroglobulin With Alzheimer DiseasePoduslo, S. E. / Shook, B. / Drigalenko, E. / Yin, X. et al. | 2002
- 36
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Carrier Testing in Fragile X Syndrome: When to Tell and TestMcConkie-Rosell, A. / Spiridigliozzi, G. A. / Sullivan, J. A. / Dawson, D. V. / Lachiewicz, A. M. et al. | 2002
- 45
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Relationship of the Delta-Opioid Receptor Gene to Heroin Abuse in a Large Chinese Case/Control SampleXu, K. / Liu, X.-H. / Nagarajan, S. / Gu, X.-Y. / Ggoldman, D. et al. | 2002
- 51
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Additional Patient With del(12)(q21.2q22): Further Evidence for a Candidate Region for Cardio-Facio-Cutaneous Syndrome?Rauen, K. A. / Albertson, D. G. / Pinkel, D. / Cotter, P. D. et al. | 2002
- 57
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Pearson Marrow-Pancreas Syndrome With Worsening Cardiac Function Caused by Pleiotropic Rearrangement of Mitochondrial DNAKrauch, G. / Wilichowski, E. / Schmidt, K. G. / Mayatepek, E. et al. | 2002
- 62
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Anticipation in Migraine With Affective PsychosisKaiser, F. et al. | 2002
- 65
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Further Delineation of the Chromosome 14q Terminal Deletion Syndromevan Karnebreek, C. D. M. / Quik, S. / Sluijter, S. / Hulsbeek, M. M. F. / Hoovers, J. M. N. / Hennekam, R. C. M. et al. | 2002
- 73
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Terminal Deletion of the Chromosome 7(q36-qter) in an Infant With Sacral Agenesis and Anterior MyelomeningoceleRodriguez, L. / Perez, I. C. / Montes, J. H. / Jareno, M. L. L. / Grondona, F. L. / Martinez-Frias, M. L. et al. | 2002
- 78
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Complete Overlap of PHACE Syndrome and Sternal Malformation - Vascular Dysplasia AssociationJames, P. A. / McGaughran, J. et al. | 2002
- 85
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A Novel Germline Point Mutation, c.2304 G→T, in Codon 768 of the RET Proto-Oncogene in a Patient With Medullary Thyroid CarcinomaAntinolo, G. / Marcos, I. / Fernandez, R. M. / Romero, M. / Borrego, S. et al. | 2002
- 195
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Testing for Genetic Associations With the PAX Gene Family in a Spina Bifida PopulationVolcik, K. A. / Blanton, S. H. / Kruzel, M. C. / Townsend, I. T. / Tyerman, G. H. / Mier, R. J. / Northrup, H. et al. | 2002
- 203
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Testing for Genetic Associations in a Spina Bifida Population: Analysis of the HOX Gene Family and Human Candidate Gene Regions Implicated by Mouse Models of Neural Tube DefectsVolcik, K. A. / Blanton, S. H. / Kruzel, M. C. / Townsend, I. T. / Tyerman, G. H. / Mier, R. J. / Northrup, H. et al. | 2002
- 208
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SNPs in the CpG Island of NAP1L2: A Possible Link Between DNA Methylation and Neural Tube Defects?Rogner, U. C. / Danoy, P. / Matsuda, F. / Moore, G. E. / Stanier, P. / Avner, P. et al. | 2002
- 215
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T Locus Shows No Evidence for Linkage Disequilibrium or Mutation in American Caucasian Neural Tube Defect FamiliesSpeer, M. C. / Melvin, E. C. / Viles, K. D. / Bauer, K. A. / Rampersaud, E. / Drake, C. / George, T. M. / Enterline, D. S. / Mackey, J. F. / Worley, G. et al. | 2002
- 219
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Heterogeneity for Congenital Generalized Lipodystrophy in Seventeen Patients From OmanRajab, A. / Heathcote, K. / Joshi, S. / Jeffery, S. / Patton, M. et al. | 2002
- 226
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Prevalence of the Fragile X Syndrome in African-AmericansCrawford, D. C. / Meadows, K. L. / Newman, J. L. / Taft, L. F. / Scott, E. / Leslie, M. / Shubek, L. / Holmgreen, P. / Yeargin-Allsopp, M. / Boyle, C. et al. | 2002
- 234
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Candidate Genes Involved in Cardiovascular Risk Factors by a Family-Based Association Study on the Island of Kosrae, Federated States of MicronesiaHan, Z. / Heath, S. C. / Shmulewitz, D. / Li, W. / Auerbach, S. B. / Blundell, M. L. / Lehner, T. / Ott, J. / Stoffel, M. / Friedman, J. M. et al. | 2002
- 243
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Expanding Phenotype of XNP Mutations: Mild to Moderate Mental RetardationYntema, H. G. / Poppelaars, F. A. / Derksen, E. / Oudakker, A. R. / van Roosmalen, T. / Jacobs, A. / Obbema, H. / Brunner, H. G. / Hamel, B. C. J. / van Bokhoven, H. et al. | 2002
- 248
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Mutations in the XPD Gene in Xeroderma Pigmentosum Group D Cell Strains: Confirmation of Genotype-Phenotype CorrelationKobayashi, T. / Uchiyama, M. / Fukuro, S. / Tanaka, K. et al. | 2002
- 253
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Familial Dysautonomia: Detection of the IKBKAP IVS20^+^6^T^-^C and R696P Mutations and Frequencies Among Ashkenazi JewsDong, J. / Edelmann, L. / Bajwa, A. M. / Kornreich, R. / Desnick, R. J. et al. | 2002
- 258
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Chromosome 13q Neocentromeres: Molecular Cytogenetic Characterization of Three Additional Cases and Clinical SpectrumLi, S. / Malafiej, P. / Levy, B. / Mahmood, R. / Field, M. / Hughes, T. / Lockhart, L. H. / Wu, Z. / Huang, M. / Hirschhorn, K. et al. | 2002
- 268
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Paternal UPD14 Is Responsible for a Distinctive Malformation ComplexKurosawa, K. / Sasaki, H. / Sato, Y. / Yamanaka, M. / Shimizu, M. / Ito, Y. / Okuyama, T. / Matsuo, M. / Imaizumi, K. / Kuroki, Y. et al. | 2002
- 273
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Mosaic Variegated Aneuploidy With Growth Hormone Deficiency and Congenital Heart DefectsLane, A. H. / Aijaz, N. / Galvin-Parton, P. / Lanman, J. / Mangano, R. / Wilson, T. A. et al. | 2002
- 278
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Clinical, Cytogenetic, and Molecular Findings in 45,X/47,XX,+18 Mosaicism: Clinical Report and Review of the LiteratureSchubert, R. / Eggermann, T. / Hofstaetter, C. / von Netzer, B. / Knopfle, G. / Schwanitz, G. et al. | 2002
- 283
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Report of a Child With Aortic Aneurysm, Orofacial Clefting, Hemangioma, Upper Sternal Defect, and Marfanoid Features: Possible PHACE SyndromeSlavotinek, A. M. / Dubovsky, E. / Dietz, H. C. / Lacbawan, F. et al. | 2002
- 289
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Novel De Novo Mutation of MADH4 / SMAD4 in a Patient With Juvenile PolyposisBurger, B. / Uhlhaas, S. / Mangold, E. / Propping, P. / Friedl, W. / Jenne, D. / Dockter, G. / Back, W. et al. | 2002
- 292
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Transposition of the Great Arteries in Asplenia and Polysplenia PhenotypesMarino, B. / Capolino, R. / Digilio, M. C. / Di Donato, R. et al. | 2002
- 295
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Counseling About CancerBaty, B. J. et al. | 2002
- 297
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No Threat to Board Certified Geneticists and Genetic CounselorsMcInerney, J. D. / Jenkins, J. et al. | 2002
- 298
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Reply to Correspondence by McInerney and JenkinsPyeritz, R. E. / Greendale, K. et al. | 2002
- 300
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Higher tPA Levels Are Associated With Apo EMeyer, M. A. et al. | 2002
- 301
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Genetic Risk Assessment in Carrier Testing for Spinal Muscular AtrophyOgino, S. / Leonard, D. G. B. / Rennert, H. / Ewens, W. J. / Wilson, R. B. et al. | 2002
- 308
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Genetic Heterogeneity of Syndromic X-Linked Recessive Microphthalmia-Anophthalmia: Is Lenz Microphthalmia a Single Disorder?Ng, D. / Hadley, D. W. / Tifft, C. J. / Biesecker, L. G. et al. | 2002
- 315
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Investigations of Micro-Organic Brain Damage (MOBD) in Heterozygotes of Metachromatic LeukodystrophyTylki-Szymanska, A. / Lugowska, A. / Chmielik, J. / Kotowicz, J. / Jakubowska-Winecka, A. / Zobel, M. / Berger, J. / Molzer, B. et al. | 2002
- 320
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Developmental Field Defects: Coming Together of Associations and Sequences During BlastogenesisHersh, J. H. / Angle, B. / Fox, T. L. / Barth, R. F. / Bendon, R. W. / Gowans, G. et al. | 2002
- 324
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Personal Experiences of Cystic Fibrosis (CF) Carrier Couples Prospectively Identified in CF FamiliesHenneman, L. / Kooij, L. / Bouman, K. / Kate, L. P. t. et al. | 2002
- 332
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Ring Chromosome 21 in a Boy and a Derivative Chromosome 21 in the Mother: Implication for Ring Chromosome FormationMuroya, K. / Yamamoto, K. / Fukushima, Y. / Ogata, T. et al. | 2002
- 338
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Childhood-Onset Ataxia: Testing for Large CAG-Repeats in SCA2 and SCA7Mao, R. / Aylsworth, A. S. / Potter, N. / Wilson, W. G. / Breningstall, G. / Wick, M. J. / Babovic-Vuksanovic, D. / Nance, M. / Patterson, M. C. / Gomez, C. M. et al. | 2002
- 346
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Refinement of the Autosomal Recessive Polycystic Kidney Disease (PKHD1) Interval and Exclusion of an EF Hand-Containing Gene as a PKHD1 Candidate GeneOnuchic, L. F. / Mrug, M. / Hou, X. / Eggermann, T. / Bergmann, C. / Zerres, K. / Avner, E. D. / Furu, L. / Somlo, S. / Nagasawa, Y. et al. | 2002
- 353
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Unbalanced Translocation (3; 5)(q26.1; p14): A Clinical ReportRossi, M. / Di Micco, P. / Perone, L. / De Brasi, D. / Guzzetta, V. / Andreucci, M. V. / Vega, G. R. / Marzano, M. G. / Iaccarino, E. / Andria, G. et al. | 2002
- 359
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Auditory Canal Atresia, Humeroscapular Synostosis, and Other Skeletal Abnormalities: Confirmation of the Autosomal Recessive "SAMS" SyndromeHeide, H. t. / Bulstra, S. K. / Reekers, A. / Schrander, J. J. P. / Schrander-Stumpel, C. T. R. M. et al. | 2002
- 365
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Novel Mutation of TBX3 in a Japanese Family With Ulnar-Mammary Syndrome: Implication for Impaired Sex DevelopmentSasaki, G. / Ogata, T. / Ishii, T. / Hasegawa, T. / Sato, S. / Matsuo, N. et al. | 2002
- 370
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Probable Identity of Goltz Syndrome and Van Allen-Myhre Syndrome: Evidence From Phenotypic EvolutionHancock, S. / Pryde, P. / Fong, C. / Brazy, J. E. / Stewart, K. / Favour, A. / Pauli, R. M. et al. | 2002
- 380
-
Possible Third Case of Lin-Gettig SyndromeHedera, P. / Innis, J. W. et al. | 2002
- 384
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Kabuki Syndrome: Report of Six Thai Children and Further Phenotypic and Genetic DelineationShotelersuk, V. / Punyashthiti, R. / Srivuthana, S. / Wacharasindhu, S. et al. | 2002
- 391
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Craniofrontonasal Syndrome and Diaphragmatic HerniaMcGaughran, J. / Rees, M. / Battin, M. et al. | 2002
- 393
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Multicolor Karyotypic Interpretation of a Heterochromatin-Associated Marker Chromosome in a Dysmorphic Girl With Developmental DelayPicker, J. D. / Cox, G. F. / Fan, Y.-S. / Darren / Fowler, J. / Weremowicz, S. / Morton, C. C. / Lee, C. et al. | 2002
- 397
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Structural and Mutational Analysis of Antiquitin as a Candidate Gene for Meniere DiseaseLynch, M. / Cameron, T. L. / Knight, M. / Kwok, T. Y. / Thomas, P. / Forrest, S. M. / Giersch, A. B. S. / Briggs, R. J. S. / Pyman, B. C. et al. | 2002
- 400
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Bilateral Hyperplasia of the Mandibular Coronoid Processes in Patients With Nevoid Basal Cell Carcinoma Syndrome: An Undescribed SignLeonardi, R. / Caltabiano, M. / Muzio, L. L. / Gorlin, R. J. / Bucci, P. / Pannone, G. / Canfora, M. / Sorge, G. et al. | 2002
- 404
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MTHFR Is Not a Risk Factor in the Development of Isolated Nonsyndromic Cleft Lip and PalateBlanton, S. H. / Patel, S. / Hecht, J. T. / Mulliken, J. B. et al. | 2002
- 406
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Evidence for a Cleft Palate Only Locus on Chromosome 4 Near MSX1Hecht, J. T. / Mulliken, J. B. / Blanton, S. H. et al. | 2002
- 408
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Resolution of Non-immune Hydrops in Noonan Syndrome With Favorable OutcomeWitters, I. / Spitz, B. / Van Hole, C. / Devriendt, K. / Fryns, J. P. / Verbek, K. et al. | 2002
- 410
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Localization of a Gene for Nonspecific X-Linked Mental Retardation (MRX 76) to Xp22.3-Xp21.3Kleefstra, T. / Yntema, H. G. / Oudakker, A. R. / de Vries, B. B. A. / van Bokhoven, H. / Hamel, B. C. J. / Poppelaars, F. A. / Ausems, M. G. E. M. et al. | 2002
- 412
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Genetics and Public Health in the 21st CenturyZlotogora, J. et al. | 2002
- 413
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Mosaic Trisomy of a Small r(1) With an Abnormal PhenotypeShanske, A. L. / Marion, R. W. et al. | 2002
- 414
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Reply to Correspondence From Shanske and Marion - "Mosaic Trisomy of a Small r(1) With an Abnormal Phenotype"Dawson, A. J. / Chudley, A. E. et al. | 2002