Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity | Genetics in Medicine
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes | European Journal of Human Genetics
Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics
Clinical and Experimental Pediatrics
Cancers | Free Full-Text | Chromosome Imbalances in Neuroblastoma—Recent Molecular Insight into Chromosome 1p-deletion, 2p-gain, and 11q-deletion Identifies New Friends and Foes for the Future
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
Deletion of genes for Fmo1, Fmo2, and Fmo4 from mouse chromosome 1. (A)... | Download Scientific Diagram
Chromosome 12 humain — Wikipédia
Clinical characterization of individuals with the distal 1q21.1 microdeletion
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate | European Journal of Human Genetics
Frontiers | Case Report: Identification of a de novo Microdeletion 1q44 in a Patient With Seizures and Developmental Delay
Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia ...
Le portrait de Thomas - délétion sur le chromosome 4 - Blog Hop'Toys
Photos of one family with 1q21.1 deletions (cases 7-9). (A) The... | Download Scientific Diagram
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25. - Abstract - Europe PMC
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles | Italian Journal of Pediatrics | Full
1q21.1 deletion or duplication
Frontiers | Case Report: Two New Cases of Chromosome 12q14 Deletions and Review of the Literature
Facial appearance of individuals with the 1q21.1 microdeletion.(a)... | Download Scientific Diagram
Chromosomes and chromosome rearrangements - ppt download
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability | Molecular Cytogenetics | Full Text
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report | BMC Pediatrics | Full Text
Chromosome 18 humain — Wikipédia
Cutis laxa in a patient with 1p36 deletion syndrome - Zhang - 2018 - The Journal of Dermatology - Wiley Online Library
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
1q4 Deletions - Unique - The Rare Chromosome Disorder Support ...
