Perinatal findings and molecular cytogenetic analyses ofde novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference16 articles.
1. , . 2000. Macrocephaly. In Fetology, , (eds). McGraw-Hill: New York; 153–157.
2. Prenatal diagnosis of Gorlin syndrome
3. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.
4. Analysis of 133 Meioses Places the Genes for Nevoid Basal Cell Carcinoma (Gorlin) Syndrome and Fanconi Anemia Group C in a 2.6-cM Interval and Contributes to the Fine Map of 9q22.3
5. Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
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1. Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate;Molecular Syndromology;2022-10-27
2. Hedgehog Signaling for Urogenital Organogenesis and Prostate Cancer: An Implication for the Epithelial–Mesenchyme Interaction (EMI);International Journal of Molecular Sciences;2019-12-20
3. Gorlin syndrome presenting with primary infertility and bilateral calcified ovarian fibromas;Journal of Obstetrics and Gynaecology;2019-04-25
4. De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay;Child Neurology Open;2019-01-01
5. De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus;Neuron;2018-07
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