1q21.1 microdeletion: MedlinePlus Genetics
1q21.1 deletion syndrome - Wikipedia
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability | Molecular Cytogenetics | Full Text
Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics
1q4 Deletions - Unique - The Rare Chromosome Disorder Support ...
Clinical characterization of individuals with the distal 1q21.1 microdeletion
Frontiers | Case Report: Identification of a de novo Microdeletion 1q44 in a Patient With Seizures and Developmental Delay
Chromosome 18 humain — Wikipédia
Le portrait de Thomas - délétion sur le chromosome 4 - Blog Hop'Toys
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes | European Journal of Human Genetics
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities | Nature Genetics
Facial appearance of individuals with the 1q21.1 microdeletion.(a)... | Download Scientific Diagram
1p36 deletion syndrome: MedlinePlus Genetics
1p36 Deletion Support & Awareness - 1p36 DSA Blog
1q21.1 deletion or duplication
vanes on X: "Bjr pr la petite Jeanne et sa maman qui recherche Enfant ou adulte atteint de délétion au niveau du chromosome 1 Que cette petite guérisse https://t.co/pLU4n7D90C" / X
Chromosomes and chromosome rearrangements - ppt download
Chromosome 12 humain — Wikipédia
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH | European Journal of Human Genetics
The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients | European Journal of Human Genetics
1q21.1 deletion syndrome - Wikipedia
