scholarly article | Q13442814 |
P2093 | author name string | Webb T | |
Vickers S | |||
Hardy C | |||
Kilpatrick M | |||
Dahlitz M | |||
P2860 | cites work | Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15 | Q24678294 |
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis | Q31165084 | ||
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome | Q33864953 | ||
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions | Q34356063 | ||
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. | Q34680586 | ||
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome | Q34718526 | ||
Chromosome 15 in floppy infants | Q35115404 | ||
Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients | Q35204517 | ||
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome | Q67484961 | ||
Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome? | Q69461711 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 478-481 | |
P577 | publication date | 1994-06-01 | |
P1433 | published in | Journal of Medical Genetics | Q14640281 |
P1476 | title | A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome | |
P478 | volume | 31 |
Q33676035 | A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome |
Q74472220 | Clinical management of a rare de novo translocation 46,X,t(Y;15) (p11.2 approximately 11.3;q11.2).ish t(Y;15)(DYZ3+,AMELY+,SNRPN+;D15Z+) found prenatally |
Q57162083 | Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13 |
Q37201174 | Prader-Willi Syndrome: Clinical and Genetic Findings |
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