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Volumn 80, Issue 3, 1998, Pages 294-295
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Prader-Willi syndrome phenotype in X chromosome anomalies: Evidence for a distinct syndrome [4]
a
a
SPE
(United States)
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Author keywords
[No Author keywords available]
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Indexed keywords
CASE REPORT;
CHILD;
CLINICAL OBSERVATION;
DISEASE ASSOCIATION;
GENE EXPRESSION;
HUMAN;
LETTER;
MALE;
PHENOTYPE;
PRADER WILLI SYNDROME;
PRIORITY JOURNAL;
SYNDROME DELINEATION;
X CHROMOSOME ABERRATION;
CHILD;
CHROMOSOME ABERRATIONS;
CHROMOSOME DISORDERS;
HUMANS;
MALE;
OBESITY;
PHENOTYPE;
PRADER-WILLI SYNDROME;
X CHROMOSOME;
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EID: 0031726172
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19981116)80:3<294::AID-AJMG24>3.0.CO;2-F Document Type: Letter |
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Times cited : (4)
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References (13)
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