Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients-Reference-Cited by-同舟云学术

Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients

Author:

Lin Angela E.¹,Traum Avram Z.²,Sahai Inderneel¹,Keppler-Noreuil Kim³,Kukolich Mary K.⁴,Adam Margaret P.⁵,Westra Sjirk J.⁶,Arts Heleen H.⁷

Affiliation:

1. Medical Genetics; MassGeneral Hospital for Children; Boston Massachusetts

2. Pediatric Nephrology Unit, Department of Pediatrics; MassGeneral Hospital for Children; Boston Massachusetts

3. Genetics Disease Research Branch, Human Development Section; National Human Genome Research Institute (NHGRI)/NIH; Bethesda Maryland

4. Clinical Genetics Service; Cook Children's Hospital; Fort Worth Texas

5. Division of Genetic Medicine; University of Washington; Seattle Washington

6. Department of Radiology; Massachusetts General Hospital; Boston Massachusetts

7. Department of Human Genetics; Radboud University Medical Centre; Nijmegen The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference38 articles.

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