FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA

MeSH terms

• Abnormalities, Severe Teratoid*
• Alopecia*
• Arm*
• Blood Group Antigens*
• Brain Diseases*
• Chromosome Aberrations*
• Chromosome Disorders*
• Chromosomes, Human, Pair 18*
• Congenital Abnormalities*
• Genetics, Medical*
• Holoprosencephaly*
• Humans
• Infant
• Intellectual Disability*
• Limbic System*