Chromosomes and chromosome rearrangements - ppt download
Common Chromosomal Disorders (Chromosomes 1-5 and X and Y)
Chromosomal disorders | Genetic Alliance UK
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
Chromosome 12 humain — Wikipédia
1q21.1 microdeletion: MedlinePlus Genetics
1q4 Deletions - Unique - The Rare Chromosome Disorder Support ...
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate | European Journal of Human Genetics
Figure 3 from Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7. | Semantic Scholar
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes | European Journal of Human Genetics
Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH - Shariati - 2018 - Clinical Case Reports - Wiley Online Library
1q21.1 deletion syndrome - Wikipedia
Clinical and Experimental Pediatrics
1p36 deletion syndrome: MedlinePlus Genetics
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity | Genetics in Medicine
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 syndrome - Wikipedia
Clinical characterization of individuals with the distal 1q21.1 microdeletion
Chromosome 18 humain — Wikipédia
1p36 Deletion Support & Awareness - 1p36 DSA Blog
Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities - ScienceDirect
1q21.1 deletion or duplication
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 ...
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
