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Page 1: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 2: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 3: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 4: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 5: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 6: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

Page 7: · Prader-WilIi syndrome Chromosome 15q14 deletion syndrome Chromosome 15q25 deletion syndrome HCD Chromosome 15q26-qter deletion syndrome Levy-Shanske syndrome Chromosome 16p deletion

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Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multi ...orca.cf.ac.uk/104397/1/Manuscript_R2_Jan4.pdf · Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS)

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PARTIAL DELETION SHORT ARMSOF A CHROMOSOME OF THE … · PARTIAL DELETION OFA 4-5 CHROMOSOME 85 Discussion Our cytological observations correspond to the findings madebyLejeuneet

DYRK1A and 21q22.13 deletion syndrome FTNW · The DYRK1A gene is on chromosome 21q22.13 and is one of the genes that is missing in the 21q22.13 deletion syndrome. When we compare

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Genetics andmedicine Velocardiofacial syndrome · deletion of chromosome 22 causing DiGeorge syndrome.6 It then became apparent that monosomy 22ql1 was an important cause of DiGeorge

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DYRK1A and 21q22.13 deletion syndrome FTNP · deletion. Broadly speaking, children with a 21q22.13 deletion have the same types of problems as are found in DYRK1A syndrome. So far,

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Universidade do Minho: Página principal · 2019. 7. 10. · Williams Syndrome (WS), a genetic disorder characterized by a deletion on chromosome 7 ql 1.22-23, has been presented

For Williams Syndrome Patients - EURORDIS · Williams Syndrome (WS) is a rare disorder, caused by a deletion in chromosome no. 7. The lost material contains approximately 20 genes,

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