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	861.	Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobands. [electronic resource] by Gómez-Carpintero García, Ana Vidal Esteban, Ana Bermejo Gómez, Amanda Púa Torrejón, Ruth Camila Producer: 20201118 In: BMJ case reports vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	862.	The tale of two genes: from next-generation sequencing to phenotype. [electronic resource] by Rohanizadegan, Mersedeh Siddharath, Aishwarya Retterer, Kyle Hung, Christina Bodamer, Olaf Producer: 20210527 In: Cold Spring Harbor molecular case studies vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	863.	Familial Russell-Silver Syndrome like Phenotype in the PCNA Domain of the [electronic resource] by Sabir, A H Ryan, G Mohammed, Z Kirk, J Kiely, N Thyagarajan, M Cole, T Publication details: Case reports in genetics 2019 In: Case reports in genetics vol. 2019 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	864.	Candidate Genes Associated with Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20. [electronic resource] by Corrêa, Thiago Venâncio, Amanda Cristina Galera, Marcial Francis Riegel, Mariluce Publication details: Case reports in genetics 2020 In: Case reports in genetics vol. 2020 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	865.	A Tanzanian Boy with Molecularly Confirmed X-Linked Adrenoleukodystrophy. [electronic resource] by Dekker, M C J Sadiq, A M Mc Larty, R Mbwasi, R M Willemsen, M A A P Waterham, H R Hamel, B C Publication details: Case reports in genetics 2019 In: Case reports in genetics vol. 2019 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	866.	Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the [electronic resource] by Al-Qattan, Mohammad M Rahbeeni, Zuhair A Al-Hassnan, Zuhair N Jarman, Abdulaziz Rafique, Atif Mahabbat, Nehal Alsufayan, Faris A S Publication details: Case reports in genetics 2020 In: Case reports in genetics vol. 2020 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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