Found: 23
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Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 284, doi. 10.1034/j.1399-0004.2000.580406.x
- By:
- Publication type:
- Article
A NEW RESTRICTION FRAGMENT LENGTH POLYMORPHISM OF THE HUMAN TNF-B GENE DETECTED BY Asp HI DIGEST.
- Published in:
- International Journal of Immunogenetics, 1992, v. 19, n. 6, p. 425, doi. 10.1111/j.1744-313X.1992.tb00086.x
- By:
- Publication type:
- Article
CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15.
- Published in:
- Prenatal Diagnosis, 1996, v. 16, n. 9, p. 837, doi. 10.1002/(SICI)1097-0223(199609)16:9<837::AID-PD956>3.0.CO;2-7
- By:
- Publication type:
- Article
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.
- Published in:
- Nature, 1987, v. 329, n. 6135, p. 153, doi. 10.1038/329153a0
- By:
- Publication type:
- Article
Molekulargenetische Diagnostik von Imprintingerkrankungen.
- Published in:
- Medizinische Genetik, 2013, v. 25, n. 1, p. 5, doi. 10.1007/s11825-012-0368-2
- By:
- Publication type:
- Article
Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinoma.
- Published in:
- 1990
- By:
- Publication type:
- journal article
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13.
- Published in:
- Cytogenetic & Genome Research, 1999, v. 87, n. 1/2, p. 125, doi. 10.1159/000015378
- By:
- Publication type:
- Article
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
- Published in:
- Cytogenetic & Genome Research, 1998, v. 81, n. 3/4, p. 247, doi. 10.1159/000015039
- By:
- Publication type:
- Article
Postovulatory aging affects dynamics of mRNA, expression and localization of maternal effect proteins, spindle integrity and pericentromeric proteins in mouse oocytes.
- Published in:
- 2016
- By:
- Publication type:
- journal article
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13.
- Published in:
- Cytogenetics & Cell Genetics, 1999, v. 87, n. 1/2, p. 125, doi. 10.1159/000015378
- By:
- Publication type:
- Article
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
- Published in:
- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 247, doi. 10.1159/000015039
- By:
- Publication type:
- Article
Molekulare Genetik und Diagnostik des Retinoblastoms Bedeutung für die Ophthalmologische Praxis *.
- Published in:
- Der Ophthalmologe, 1997, v. 94, n. 4, p. 263, doi. 10.1007/s003470050110
- By:
- Publication type:
- Article
Imprinting defects on human chromosome 15.
- Published in:
- Cytogenetic & Genome Research, 2006, v. 113, n. 1-4, p. 292, doi. 10.1159/000090844
- By:
- Publication type:
- Article
Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma.
- Published in:
- Human Mutation, 1998, v. 12, n. 6, p. 434, doi. 10.1002/(SICI)1098-1004(1998)12:6<434::AID-HUMU16>3.0.CO;2-7
- By:
- Publication type:
- Article
The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder.
- Published in:
- 2009
- By:
- Publication type:
- Journal Article
The European Prader–Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder.
- Published in:
- Journal of Intellectual Disability Research, 2009, v. 53, n. 6, p. 538, doi. 10.1111/j.1365-2788.2009.01172.x
- By:
- Publication type:
- Article
Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 6, p. 1011, doi. 10.1093/hmg/7.6.1011
- By:
- Publication type:
- Article
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 9, p. 784
- By:
- Publication type:
- Article
A study of DNA polymorphisms around the human apolipoprotein Al gene in hyperlipidaemic and normal individuals.
- Published in:
- Clinical Genetics, 1985, v. 28, n. 4, p. 296, doi. 10.1111/j.1399-0004.1985.tb00403.x
- By:
- Publication type:
- Article
Genomisches Imprinting und Imprintingfehler.
- Published in:
- Medizinische Genetik, 2010, v. 22, n. 4, p. 385, doi. 10.1007/s11825-010-0244-x
- By:
- Publication type:
- Article
Uwe Claussen (1945–2008).
- Published in:
- Medizinische Genetik, 2008, v. 20, n. 3, p. 332, doi. 10.1007/s11825-008-0128-5
- By:
- Publication type:
- Article
Comment on: Jowett et al. (2010) Genetic variation at the FTO locus influences RBL2 gene expression. Diabetes;59:726-732.
- Published in:
- 2010
- By:
- Publication type:
- Letter