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rubinstein taybi syndrome

Facial dysmorphism, skeletal anomalies, congenital glucoma

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Facial dysmorphism, skeletal anomalies, congenital glucoma
Clinical phenotype of family BDCS1. The facial features of BDCS1-17 at
Facial dysmorphism, skeletal anomalies, congenital glucoma
Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
Facial dysmorphism, skeletal anomalies, congenital glucoma
Infantile glaucoma in Rubinstein–Taybi syndrome
Facial dysmorphism, skeletal anomalies, congenital glucoma
Axenfeld-Rieger syndrome: more than meets the eye
Facial dysmorphism, skeletal anomalies, congenital glucoma
Facial dysmorphism, including prominent eyes with a proptotic
Facial dysmorphism, skeletal anomalies, congenital glucoma
Hallermann Streiff Syndrome - an overview
Facial dysmorphism, skeletal anomalies, congenital glucoma
Dysmorphic features (triangular-shaped face with prominent forehead and
Facial dysmorphism, skeletal anomalies, congenital glucoma
The skeletal dysplasias
Facial dysmorphism, skeletal anomalies, congenital glucoma
Skeletal Dysplasias - Endotext - NCBI Bookshelf
Facial dysmorphism, skeletal anomalies, congenital glucoma
Patient 1 with SHORT syndrome demonstrating short stature
Facial dysmorphism, skeletal anomalies, congenital glucoma
Genes, Free Full-Text
Facial dysmorphism, skeletal anomalies, congenital glucoma
Frank-Ter Haar Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Facial dysmorphism, skeletal anomalies, congenital glucoma
Skeletal Dysplasias - Endotext - NCBI Bookshelf
Facial dysmorphism, skeletal anomalies, congenital glucoma
Secondary Childhood glaucoma – a rare association in Seckel syndrome - Manju R Pillai, Srilekha Pallamparthy, Subathra Gnanavelu, 2023
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