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
Chromosomes and chromosome rearrangements - ppt download
Facial appearance of individuals with the 1q21.1 microdeletion.(a)... | Download Scientific Diagram
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities | Nature Genetics
Chromosome 12 humain — Wikipédia
Figure 3 from Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7. | Semantic Scholar
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
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report | BMC Pediatrics | Full Text
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
1p36 deletion syndrome: MedlinePlus Genetics
Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities - ScienceDirect
1q21.1 deletion syndrome - Wikipedia
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 microdeletion: MedlinePlus Genetics
Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics
Le portrait de Thomas - délétion sur le chromosome 4 - Blog Hop'Toys
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
Clinical features of the 2q23.1 deletion syndrome. (a) Case 1, SMS185... | Download Scientific Diagram
1q4 Deletions - Unique - The Rare Chromosome Disorder Support ...
1q21.1 deletion or duplication
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH | European Journal of Human Genetics
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes | European Journal of Human Genetics
Chromosome 18 humain — Wikipédia
