Distal Limb Defects and Aplasia Cutis: Adams–Oliver Syndrome - ScienceDirect
Adams-Oliver syndrome and isolated aplasia cutis congenita in two siblings
Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome - ScienceDirect
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects - Snape - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Case report and review of literature of a rare congenital disorder: Adams-Oliver syndrome | BMC Anesthesiology | Full Text
Cornelia de Lange syndrome: MedlinePlus Genetics
Adams-Oliver syndrome: MedlinePlus Genetics
A girl with Adams Oliver syndrome. She had terminal transverse limb... | Download Scientific Diagram
Adams–Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations - Jones - 2017 - Pediatric Dermatology - Wiley Online Library
Adams-Oliver syndrome: MedlinePlus Genetics
Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams–Oliver Syndrome With Variable Cardiac Anomalies | Circulation: Cardiovascular Genetics
Adams-Oliver syndrome: MedlinePlus Genetics
Adams-Oliver Syndrome: Limited Expression | SpringerLink
Adams-Oliver syndrome - Dermatology Advisor
Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort - Meester - 2018 - Human Mutation - Wiley Online Library
Adams–Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations - Jones - 2017 - Pediatric Dermatology - Wiley Online Library
Characteristic features of Adams–Oliver syndrome present in our set of... | Download Scientific Diagram
Syndrome d'Adams-Oliver et cutis marmorata telangiectatica congenita - ScienceDirect
Mutations in NOTCH1 Cause Adams-Oliver Syndrome - ScienceDirect
Medicowesome: Medipicsowesome: Adams Oliver syndrome
Adams-Oliver syndrome: MedlinePlus Genetics
Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
![Figure 2. [(A) T2-weighted sequences of the...]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK26373/bin/thctd-Image002.jpg "Figure 2. [(A) T2-weighted sequences of the...]. - GeneReviews® - NCBI Bookshelf")
Figure 2. [(A) T2-weighted sequences of the...]. - GeneReviews® - NCBI Bookshelf
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome | Journal of Human Genetics
Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
