Concept of Twin Spotting (English)
- New search for: Koopman, R. J. J.
- New search for: Koopman, R. J. J.
- New search for: Effendy, I.
In:
Mosaicism in Human Skin
4
;
355-358
;
1999
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ISSN:
- Article (Journal) / Print
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Title:Concept of Twin Spotting
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Contributors:Koopman, R. J. J. ( author ) / Effendy, I.
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Published in:Mosaicism in Human Skin , 4 ; 355-358AMERICAN JOURNAL OF MEDICAL GENETICS ; 85, 4 ; 355-358
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Publisher:
- New search for: JOHN WILEY & SONS LTD
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Publication date:1999-01-01
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Size:4 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 85, Issue 4
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.
- 324
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Functional X-Chromosomal Mosaicism of the Skin: Rudolf Happle and the Lines of Alfred BlaschkoTraupe, H. et al. | 1999
- 330
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Cytogenetic and Molecular Evidence for Cutaneous Mosaicism: The Ectodermal Origin of Blaschko LinesMoss, C. et al. | 1999
- 334
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Acquired Blaschkolinear DermatosesGrosshans, E. M. et al. | 1999
- 338
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Extracutaneous Analogies of Blaschko LinesRott, H.-D. et al. | 1999
- 342
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Cutaneous Mosaicism of Lethal MutationsHamm, H. et al. | 1999
- 346
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Hypomelanosis of Ito: No Entity, but a Cutaneous Sign of MosaicismKuster, W. / Koenig, A. et al. | 1999
- 351
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Segmental Forms of Autosomal Dominant Skin Disorders: The Puzzle of MosaicismItin, P. H. / Buechner, S. A. et al. | 1999
- 355
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Concept of Twin SpottingKoopman, R. J. J. et al. | 1999
- 359
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Paradominant Inheritance, a Hypothesis Explaining Occasional Familial Occurrence of Sporadic SyndromesSteijlen, P. M. / Van Steensel, M. A. M. et al. | 1999
- 361
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Revertant Mosaicism in Human Genetic DisordersJonkman, M. F. et al. | 1999
- 365
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Linear Lesions Reflecting Lyonization in Women Heterozygous for IFAP Syndrome (Ichthyosis Follicularis With Atrichia and Photophobia)Konig, A. / Happle, R. et al. | 1999
- 369
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Risk of Abnormal Pregnancy Outcome in Carriers of Balanced Reciprocal Translocations Involving the Miller-Dieker Syndrome (MDS) Critical Region in Chromosome 17p13.3Pollin, T. I. / Dobyns, W. B. / Crowe, C. A. / Ledbetter, D. H. / Bailey-Wilson, J. E. / Smith, A. C. M. et al. | 1999
- 376
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Down Syndrome in a Population of Elderly Mentally Retarded Patients: Genetic-Diagnostic Survey and Implications for Medical CareVan Buggenhout, G. J. C. M. / Trommelen, J. C. M. / Schoenmaker, A. / De Bal, C. / Verbeek, J. J. M. C. / Smeets, D. F. C. M. / Ropers, H. H. / Devriendt, K. / Hamel, B. C. J. / Fryns, J. P. et al. | 1999
- 385
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Neocentromere at 13q32 in One of Two Stable Markers Derived From a 13q21 BreakRivera, H. / Vasquez, A. I. / Garcia-Cruz, D. / Crolla, J. A. et al. | 1999
- 389
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"Essentially Pure" Partial Trisomy (6)(p23->pter) in Two Brothers Due to Maternal t(6;17)(p23;p13.3)Roethlisberger, B. / Kotzot, D. / Gnehm, H. E. / Schinzel, A. et al. | 1999
- 395
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Congenital Hypertrichosis, Osteochondrodysplasia, and Cardiomegaly: Cantu SyndromeRobertson, S. U. / Kirk, E. / Bernier, F. / Brereton, J. / Turner, A. / Bankier, A. et al. | 1999
- 403
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Trisomy 20p Resulting From Inverted Duplication and Neocentromere FormationVoullaire, L. / Saffery, R. / Davies, J. / Earle, E. / Kalitsis, P. / Slater, H. / Irvine, D. V. / Choo, K. H. A. et al. | 1999
- 409
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Tibial Hemimelia in Langer-Giedion Syndrome - Possible Gene Location for Tibial Hemimelia at 8qStevens, C. A. / Moore, C. A. et al. | 1999
- 413
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Clinical and Molecular Studies of Brachydactyly Type DRobin, N. H. / Hurvitz, J. / Warman, M. L. / Morrison, S. et al. | 1999
- 419
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Ventricular Noncompaction and Distal Chromosome 5q DeletionPauli, R. M. / Scheib-Wixted, S. / Gripe, L. / Izumo, S. / Sekhon, G. S. et al. | 1999
- 424
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Letter to the Editor: Mosaicism in Prader-Willi Syndrome: Detection Using Fluorescent In Situ HybridizationGolden, W. L. / Sudduth, K. W. / Burnett, S. H. / Kelly, T. E. et al. | 1999
- 426
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Clarification of a Diagnosis of IPRoberts, J. L. et al. | 1999
- 427
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Reply to the Letter to the Editor by Landau Roberts - "Clarification of a Diagnosis of IP"Scheuerle, A. et al. | 1999