Works matching IS 15524868 AND DT 2018 AND VI 178 AND IP 4
Results: 13
Cover Image, Volume 178, Number 4, December 2018.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. i, doi. 10.1002/ajmg.c.31674
- Publication type:
- Article
Hallermann–Streiff syndrome: A missing molecular link for a highly recognizable syndrome.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 398, doi. 10.1002/ajmg.c.31668
- By:
- Publication type:
- Article
An update on oculocerebrocutaneous (Delleman‐Oorthuys) syndrome.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 414, doi. 10.1002/ajmg.c.31667
- By:
- Publication type:
- Article
Rhombencephalosynapsis: Fused cerebellum, confused geneticists.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 432, doi. 10.1002/ajmg.c.31666
- By:
- Publication type:
- Article
Unsolved recognizable patterns of human malformation: Challenges and opportunities.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 382, doi. 10.1002/ajmg.c.31665
- By:
- Publication type:
- Article
The etiology of VACTERL association: Current knowledge and hypotheses.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 440, doi. 10.1002/ajmg.c.31664
- By:
- Publication type:
- Article
The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 458, doi. 10.1002/ajmg.c.31662
- By:
- Publication type:
- Article
Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 387, doi. 10.1002/ajmg.c.31661
- By:
- Publication type:
- Article
Nablus syndrome: Easy to diagnose yet difficult to solve.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 447, doi. 10.1002/ajmg.c.31660
- By:
- Publication type:
- Article
PHACE syndrome: Infantile hemangiomas associated with multiple congenital anomalies: Clues to the cause.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 407, doi. 10.1002/ajmg.c.31659
- By:
- Publication type:
- Article
Aicardi syndrome, an unsolved mystery: Review of diagnostic features, previous attempts, and future opportunities for genetic examination.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 423, doi. 10.1002/ajmg.c.31658
- By:
- Publication type:
- Article
Publication schedule for 2018.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 381, doi. 10.1002/ajmg.c.31582
- Publication type:
- Article
Table of Contents, Volume 178, Number 4, December 2018.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 4, p. 379, doi. 10.1002/ajmg.c.31581
- Publication type:
- Article