| scholarly article | Q13442814 |
| P2093 | author name string | M G Butler | |
| P2860 | cites work | Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome | Q33864953 |
| Is Angelman syndrome an alternate result of del(15)(q11q13)? | Q34187549 | ||
| The Angelman ("happy puppet") syndrome | Q34278541 | ||
| Hypopigmentation in the Prader-Willi syndrome | Q35199084 | ||
| Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases | Q35202068 | ||
| Recurrence risk in the Angelman ("happy puppet") syndrome | Q39688903 | ||
| Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis | Q40178026 | ||
| Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome | Q42463969 | ||
| Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation. | Q48332243 | ||
| Plasma immunoreactive beta-melanocyte stimulating hormone (lipotropin) levels in individuals with Prader-Labhart-Willi syndrome. | Q51627675 | ||
| Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion | Q69461724 | ||
| Rapid radioimmunoassay for corticotropin in unextracted human plasma | Q70183954 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 140-146 | |
| P577 | publication date | 1989-07-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome | |
| P478 | volume | 45 |
| Q55044754 | A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13. |
| Q43057916 | AMINO ACID LEVELS IN PRADER-WILLI SYNDROME AND OBESE INDIVIDUALS. |
| Q28247810 | Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy |
| Q38830153 | Benefits and limitations of prenatal screening for Prader-Willi syndrome |
| Q54247701 | Clinical and genetic features of Prader-Willi syndrome in China. |
| Q35100466 | Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. |
| Q37203690 | EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME. |
| Q36148677 | Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse |
| Q33752509 | Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome |
| Q34680586 | Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. |
| Q40026342 | Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment. |
| Q73494617 | Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele |
| Q52170199 | Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes. |
| Q34719918 | Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? |
| Q59798952 | Multimodal imaging in a patient with Prader-Willi syndrome |
| Q37201174 | Prader-Willi Syndrome: Clinical and Genetic Findings |
| Q37229655 | Prader-Willi Syndrome: Genetics and Behavior |
| Q34229319 | Prader-Willi Syndrome: Obesity due to Genomic Imprinting |
| Q24517941 | Prader-Willi syndrome |
| Q51886650 | Prader-Willi syndrome. |
| Q36240989 | Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings |
| Q34061685 | Prader-Willi syndrome: consensus diagnostic criteria. |
| Q33858951 | Prader-Willi syndrome: current understanding of cause and diagnosis |
| Q41585963 | Prader-willi syndrome: clinical aspects |
| Q68325740 | Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome |
| Q52043084 | The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. |
| Q36236002 | The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito. |
| Q67514407 | The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region |
| Q24669671 | The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12 |
| Q24656270 | Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene |
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