Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene

Keyphrases

• Diaphragmatic Hernia 100%
• Chromosomal Deletion 100%
• DEL-1 100%
• Human Ferritin 100%
• Ferritin Genes 100%
• Chromosome 1 66%
• Genital 33%
• Long Arm 33%
• Paucity 33%
• Hypoplasia 33%
• Subcutaneous Tissue 33%
• Renin 33%
• Human Genes 33%
• 46,XY 33%
• Gene Mapping 33%
• Genomic DNA (gDNA) 33%
• Severe Respiratory Failure 33%
• Restriction Analysis 33%
• Karyotype Analysis 33%
• Glucocerebrosidase 33%
• Regional Mapping 33%
• H Subunit 33%
• Interstitial Deletion 33%
• Facial Dysmorphism 33%
• Flexion Contracture 33%
• H4 Histones 33%
• α-spectrin 33%

Medicine and Dentistry

• Diaphragm Hernia 100%
• Ferritin 100%
• Chromosome Deletion 100%
• Neonatal Infant 66%
• Karyotype 66%
• Chromosome 1 66%
• Hypoplasia 33%
• Neck 33%
• Subcutaneous Tissue 33%
• Arm 33%
• Respiratory Distress 33%
• Genomic DNA 33%
• Histone H4 33%
• Finger 33%
• Restriction Mapping 33%
• Renin 33%
• Glucosylceramidase 33%
• Gene Map 33%
• Flexion Contracture 33%
• Fodrin 33%