| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-8628(19960409)67:2<229::AID-AJMG17>3.0.CO;2-L |
| P698 | PubMed publication ID | 8723054 |
| P50 | author | Markus M Nöthen | Q37634364 |
| P2093 | author name string | Wolf HK | |
| Cichon S | |||
| Propping P | |||
| P2860 | cites work | Mosaic and polymorphic imprinting of the WT1 gene in humans | Q48084685 |
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. | Q54612233 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| The D4 dopamine receptor (DRD4) maps to distal 11p close to HRAS | Q57419003 | ||
| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
| Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome | Q24305283 | ||
| Cloning of the gene for a human dopamine D4 receptor with high affinity for the antipsychotic clozapine | Q24319813 | ||
| Multiple dopamine D4 receptor variants in the human population | Q24336675 | ||
| Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism | Q24337027 | ||
| Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 | ||
| A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 | ||
| Monoallelic expression of the human H19 gene | Q28184725 | ||
| Parental imprinting of the human H19 gene | Q28187996 | ||
| Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region | Q28242397 | ||
| Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2 | Q31158518 | ||
| Identification of a novel paternally expressed gene in the Prader-Willi syndrome region | Q34318139 | ||
| Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patients. | Q34346884 | ||
| Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome | Q41523994 | ||
| Dopamine D4 receptor variant, D4GLYCINE194, in Africans, but not in Caucasians: no association with schizophrenia | Q44743600 | ||
| Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity | Q48077428 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 229-231 | |
| P577 | publication date | 1996-04-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | Lack of imprinting of the human dopamine D4 receptor (DRD4) gene | |
| P478 | volume | 67 |
| Q28209960 | Biallelic expression of HRAS and MUCDHL in human and mouse |
| Q44137047 | Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4. |
| Q39058741 | Epigenetic repression of the dopamine receptor D4 in pediatric tumors of the central nervous system |
| Q33313877 | Gene expression profile of neuronal progenitor cells derived from hESCs: activation of chromosome 11p15.5 and comparison to human dopaminergic neurons. |
| Q38671578 | Obsessive-compulsive disorder, which genes? Which functions? Which pathways? An integrated holistic view regarding OCD and its complex genetic etiology |
| Q28298778 | Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders |
| Q30168689 | The dopamine D(4) receptor: one decade of research |
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