Pages that link to "Q33864953"
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The following pages link to Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (Q33864953):
Displaying 50 items.
- A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism (Q24655126) (← links)
- Genomics and autism spectrum disorder (Q27015042) (← links)
- Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region (Q28208127) (← links)
- Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy (Q28247810) (← links)
- Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology (Q28263222) (← links)
- Decreased bone mineral density in Prader-Willi syndrome: comparison with obese subjects (Q28366548) (← links)
- Genomic imprinting: review and relevance to human diseases. (Q30501672) (← links)
- Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype (Q33592964) (← links)
- On the parental origin of de novo mutation in man. (Q33596715) (← links)
- Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome (Q33596746) (← links)
- Molecular and cytogenetic studies of the Prader-Willi syndrome (Q33597595) (← links)
- DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome (Q33675694) (← links)
- A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome (Q33676035) (← links)
- The value of the study of natural history in genetic disorders and congenital anomaly syndromes (Q33676984) (← links)
- Microdeletion syndromes, balanced translocations, and gene mapping (Q33676997) (← links)
- Alagille syndrome (Q33678457) (← links)
- Molecular screening for proximal 15q abnormalities in a mentally retarded population (Q33680953) (← links)
- Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome (Q33776638) (← links)
- Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992. (Q33776657) (← links)
- From microscopes to microarrays: dissecting recurrent chromosomal rearrangements (Q33805828) (← links)
- Prader-Willi syndrome: current understanding of cause and diagnosis (Q33858951) (← links)
- Robinow syndrome: report of two patients and review of literature (Q33860252) (← links)
- An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene. (Q33860275) (← links)
- Genomics, intellectual disability, and autism (Q33937230) (← links)
- Three probands with autistic disorder and isodicentric chromosome 15. (Q33970872) (← links)
- Prader-Willi syndrome: consensus diagnostic criteria. (Q34061685) (← links)
- Prader-Willi Syndrome: Obesity due to Genomic Imprinting (Q34229319) (← links)
- INTRAFAMILIAL AND MIDPARENTAL-CHILD CORRELATIONS AND HERITABILITY ESTIMATES OF ANTHROPOMETRIC MEASUREMENTS IN PRADER-WILLI SYNDROME FAMILIES. (Q34653107) (← links)
- Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. (Q34680586) (← links)
- Growth standards of infants with Prader-Willi syndrome (Q34725740) (← links)
- Psychiatric disorders in Prader-Willi syndrome: epidemiology and management (Q35078275) (← links)
- Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. (Q35100466) (← links)
- Mutational risks in females: genomic imprinting and maternal molecules (Q35148451) (← links)
- Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome. (Q35197277) (← links)
- Parental origin of de novo constitutional deletions of chromosomal band 11p13 (Q35198154) (← links)
- Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers (Q35198215) (← links)
- Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3. (Q35198409) (← links)
- Hypopigmentation in the Prader-Willi syndrome (Q35199084) (← links)
- Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients (Q35204517) (← links)
- Isolation and analysis of DNA markers specific to human chromosome 15. (Q35245692) (← links)
- On the origin of chromosome anomaly (Q35245848) (← links)
- Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q. (Q35248500) (← links)
- The genetics of microdeletion and microduplication syndromes: an update. (Q35765523) (← links)
- Differentiated recurrence risk estimations in the Prader-Willi syndrome (Q36291111) (← links)
- Angelman syndrome: clinical profile (Q36340020) (← links)
- Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice (Q36554182) (← links)
- Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation (Q36846020) (← links)
- A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes (Q37060687) (← links)
- Prader-Willi Syndrome: Clinical and Genetic Findings (Q37201174) (← links)
- RESTING METABOLIC RATE IN PRADER-WILLI SYNDROME (Q37210799) (← links)