A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome

scientific article published on June 1994

A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1136/JMG.31.6.478
P932PMC publication ID1049927
P698PubMed publication ID8071975
P5875ResearchGate publication ID15127223

P2093author name stringWebb T
Vickers S
Hardy C
Kilpatrick M
Dahlitz M
P2860cites workLocalization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15Q24678294
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisQ31165084
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndromeQ33864953
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 regionsQ34356063
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.Q34680586
Deletions of chromosome 15 as a cause of the Prader-Willi syndromeQ34718526
Chromosome 15 in floppy infantsQ35115404
Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patientsQ35204517
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndromeQ67484961
Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?Q69461711
P433issue6
P407language of work or nameEnglishQ1860
P304page(s)478-481
P577publication date1994-06-01
P1433published inJournal of Medical GeneticsQ14640281
P1476titleA male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome
P478volume31

Reverse relations

cites work (P2860)
Q33676035A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome
Q74472220Clinical 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
Q57162083Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13
Q37201174Prader-Willi Syndrome: Clinical and Genetic Findings

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