Angular Homeostasis IX. Polygonal Orbits With a Moving Target: Implications for Anomalous Numbers of Digits in Congenital Heart Disease (Unknown)
- New search for: Murphy, E. A.
- New search for: Murphy, E. A.
In:
AMERICAN JOURNAL OF MEDICAL GENETICS
;
45
, 3
;
383
;
1993
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ISSN:
- Article (Journal) / Print
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Title:Angular Homeostasis IX. Polygonal Orbits With a Moving Target: Implications for Anomalous Numbers of Digits in Congenital Heart Disease
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Contributors:Murphy, E. A. ( author )
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Published in:AMERICAN JOURNAL OF MEDICAL GENETICS ; 45, 3 ; 383
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Publisher:
- New search for: JOHN WILEY & SONS LTD
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Publication date:1993-01-01
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Size:383 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:Unknown
- New search for: 616.042
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616.042 -
Source:
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Table of contents – Volume 45, Issue 3
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.
- 285
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Marden-Walker Phenotype: Spectrum of Variability in Three InfantsRamer, J. C. / Frankel, C. A. / Ladda, R. L. et al. | 1993
- 292
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Brief Clinical Report: Long Term Survival of an Infant With SirenomeliaClarke, L. A. / Stringer, D. A. / Fraser, G. C. / Siu Li Yong et al. | 1993
- 297
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Phocomelia, Oligodactyly, and Acrania: The Schinzel-Phocomelia SyndromeChitayat, D. / Stalker, H. J. / Vekemans, M. / Delneste, D. et al. | 1993
- 300
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Pfeiffer Syndrome Update, Clinical Subtypes, and Guidelines for Differential DiagnosisCohen, M. M. et al. | 1993
- 308
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Confirmation That the Velo-Cardio-Facial Syndrome Is Associated With Haplo-Insufficiency of Genes at Chromosome 22q11Kelly, D. / Goldberg, R. / Wilson, D. / Lindsay, E. et al. | 1993
- 313
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Velo-Cardio-Facial Syndrome: A Review of 120 PatientsGoldberg, R. / Motzkin, B. / Marion, R. / Scambler, P. J. et al. | 1993
- 320
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Spondylo-Meta-Epiphyseal Dysplasia (SMED), Short Limb-Hand Type: A Congenital Familial Skeletal Dysplasia With Distinctive Features and HistopathologyBorochowitz, Z. / Langer, L. O. / Gruber, H. E. / Lachman, R. et al. | 1993
- 327
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Barth Syndrome: Clinical Features and Confirmation of Gene Localisation to Distal Xq28Ades, L. C. / Gedeon, A. K. / Wilson, M. J. / Latham, M. et al. | 1993
- 335
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Trimethylaminuria in a Girl With Prader-Willi Syndrome and del(15)(q11q13)Chen, H. / Aiello, F. et al. | 1993
- 340
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Familial Mediterranean Fever in the Colchicine Era: The Fate of One FamilyZemer, D. / Livneh, A. / Pras, M. / Sohar, E. et al. | 1993
- 345
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Exclusion of Type II and Type VI Procollagen Gene Mutations in a Five-Generation Family With Multiple Epiphyseal DysplasiaWeaver, E. J. / Summerville, G. P. / Yeh, G. / Hervada-Page, M. et al. | 1993
- 353
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Microcephaly and Digital Anomalies: A Newly Recognized Syndrome of Recessively Inherited Mental RetardationKelly, T. E. / Kirson, L. / Wyatt, J. et al. | 1993
- 356
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Brief Clinical Report: Elevated Human Chorionic Gonadotropin Levels in Pregnancies With Sex Chromosome AbnormalitiesBarnes-Kedar, I. / Amiel, A. / Maor, O. / Fejgin, M. et al. | 1993
- 358
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Syndrome of Cleft Palate, Microcephaly, Large Ears, and Short Stature (Say Syndrome)Abu-Libdeh, B. / Fujimoto, A. / Ehinger, M. et al. | 1993
- 361
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Chorionic Villus Sampling Followed by Amniocentesis in the Same PregnancyDonnenfeld, A. E. / Librizzi, R. J. / Dunn, L. K. / Craparo, F. et al. | 1993
- 365
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Unbalanced Mosaic Karyotypes With Different Structural Abnormalities Involving a Common Chromosome Region: Report of Two CasesPettenati, M. J. / Teot, L. A. / Smith, C. / Hayworth, R. et al. | 1993
- 370
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Brief Clinical Report: Michelin Tire Baby Syndrome: Familial Constriction Bands During Infancy and Early Childhood in Four GenerationsBass, H. N. / Caldwell, S. / Brooks, B. S. et al. | 1993
- 373
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Extended Major Histocompatibility Complex Haplotypes in Celiac Patients in the West of IrelandMannion, A. / Stevens, F. M. / McCarthy, C. F. / Grimes-O'Cearbhaill, H. et al. | 1993
- 378
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Prenatal Diagnosis of Tetraploidy: A Case ReportCoe, S. J. / Kapur, R. / Luthardt, F. / Rabinovitch, P. et al. | 1993
- 383
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Angular Homeostasis IX. Polygonal Orbits With a Moving Target: Implications for Anomalous Numbers of Digits in Congenital Heart DiseaseMurphy, E. A. et al. | 1993
- 392
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Birth Prevalence Study of the Apert SyndromeCzeizel, A. E. / Elek, C. / Susanszky, E. et al. | 1993
- 394
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Screening for Chromosome AbnormalitiesBogart, M. H. et al. | 1993
- 395
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Maternal Age and Recommendation of AmniocentesisReynolds, T. / Dawson, A. et al. | 1993
- 397
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Ankyloblepharon Filiforme Adnatum and Imperforate AnusAughton, D. J. / Hufnagle, K. G. et al. | 1993
- 398
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Prolonged Maternal Diet Imbalance and Recurrent Fetuses With Congenital AnomaliesSheffer, R. N. / Shohat, M. / Merlob, P. et al. | 1993
- 401
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Decrease in the Size of the Myotonic Dystrophy CTG Repeat During Transmission From Parent to Child: Implications for Genetic Counselling and Genetic AnticipationHunter, A. G. W. / Jacob, P. / O'Hoy, K. / MacDonald, I. et al. | 1993
- 408
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Presymptomatic Diagnosis of SMA III by Genotype AnalysisBrahe, C. / Zappata, S. / Velona, I. / Bertini, E. et al. | 1993