Nablus syndrome: Easy to diagnose yet difficult to solve (English)
- New search for: Allanson, Judith
- New search for: Smith, Amanda
- New search for: Forzano, Francesca
- New search for: Lin, Angela E.
- New search for: Raas‐Rothschild, Annick
- New search for: Howley, Heather E.
- New search for: Boycott, Kym M.
- New search for: Allanson, Judith
- New search for: Smith, Amanda
- New search for: Forzano, Francesca
- New search for: Lin, Angela E.
- New search for: Raas‐Rothschild, Annick
- New search for: Howley, Heather E.
- New search for: Boycott, Kym M.
In:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
;
178
, 4
;
447-457
;
2018
- Article (Journal) / Electronic Resource
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Title:Nablus syndrome: Easy to diagnose yet difficult to solve
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Contributors:Allanson, Judith ( author ) / Smith, Amanda ( author ) / Forzano, Francesca ( author ) / Lin, Angela E. ( author ) / Raas‐Rothschild, Annick ( author ) / Howley, Heather E. ( author ) / Boycott, Kym M. ( author )
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Published in:American Journal of Medical Genetics Part C: Seminars in Medical Genetics ; 178, 4 ; 447-457
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Publisher:
- New search for: John Wiley & Sons, Inc.
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Publication date:2018-12-01
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Size:11 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 178, 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.
- 379
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Table of Contents, Volume 178, Number 4, December 2018| 2018
- 381
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Publication schedule for 2018| 2018
- 382
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Unsolved recognizable patterns of human malformation: Challenges and opportunitiesBoycott, Kym M. / Dyment, David A. / Innes, A. Micheil et al. | 2018
- 387
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Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further researchInnes, A. Micheil / McInnes, Brenda L. / Dyment, David A. et al. | 2018
- 398
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Hallermann–Streiff syndrome: A missing molecular link for a highly recognizable syndromeSchmidt, Julia / Wollnik, Bernd et al. | 2018
- 407
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PHACE syndrome: Infantile hemangiomas associated with multiple congenital anomalies: Clues to the causeSiegel, Dawn H. et al. | 2018
- 414
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An update on oculocerebrocutaneous (Delleman‐Oorthuys) syndromeMoog, Ute / Dobyns, William B. et al. | 2018
- 423
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Aicardi syndrome, an unsolved mystery: Review of diagnostic features, previous attempts, and future opportunities for genetic examinationWong, Bibiana K. Y. / Sutton, V. Reid et al. | 2018
- 432
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Rhombencephalosynapsis: Fused cerebellum, confused geneticistsAldinger, Kimberly A. / Dempsey, Jennifer C. / Tully, Hannah M. / Grout, Megan E. / Mehaffey, Michele G. / Dobyns, William B. / Doherty, Dan et al. | 2018
- 440
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The etiology of VACTERL association: Current knowledge and hypothesesSolomon, Benjamin D. et al. | 2018
- 447
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Nablus syndrome: Easy to diagnose yet difficult to solveAllanson, Judith / Smith, Amanda / Forzano, Francesca / Lin, Angela E. / Raas‐Rothschild, Annick / Howley, Heather E. / Boycott, Kym M. et al. | 2018
- 458
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The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®Hartley, Taila / Balcı, Tuğçe B. / Rojas, Samantha K. / Eaton, Alison / Canada, Care4Rare / Dyment, David A. / Boycott, Kym M. et al. | 2018
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Cover Image, Volume 178, Number 4, December 2018| 2018