Search
| Leader | 00000nz a2200037n 45 0 | ||
|---|---|---|---|
| 001 | WKP|Q87803443 (VIAF cluster) (Authority/Source Record) | ||
| 003 | WKP | ||
| 005 | 20241221010736.0 | ||
| 008 | 241221nneanz||abbn n and d | ||
| 035 | ‡a (WKP)Q87803443 | ||
| 024 | ‡a 0000-0002-0216-3909 ‡2 orcid | ||
| 035 | ‡a (OCoLC)Q87803443 | ||
| 100 | 0 | ‡a অ্যালিসন ফস্টার ‡9 bn | |
| 400 | 0 | ‡a Alison Foster ‡c researcher ‡9 en | |
| 400 | 0 | ‡a A Foster ‡c wetenschapper ‡9 nl | |
| 670 | ‡a Author's Kosaki overgrowth syndrome: a novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications | ||
| 670 | ‡a Author's Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patients | ||
| 670 | ‡a Author's Patient understanding of genetic information influences reproductive decision making in retinoblastoma. | ||
| 670 | ‡a Author's The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients | ||
| 670 | ‡a Author's The phenotype of Sotos syndrome in adulthood: A review of 44 individuals | ||
| 909 | ‡a (orcid) 0000000202163909 ‡9 1 | ||
| 919 | ‡a phenotypeofsotossyndromeinadulthoodareviewof44individuals ‡A The phenotype of Sotos syndrome in adulthood: A review of 44 individuals ‡9 1 | ||
| 919 | ‡a patientunderstandingofgeneticinformationinfluencesreproductivedecisionmakinginretinoblastoma ‡A Patient understanding of genetic information influences reproductive decision making in retinoblastoma. ‡9 1 | ||
| 919 | ‡a nullvariantsanddeletionsinbrwd3causean10linkedsyndromeofmildmoderateintellectualdisabilitymacrocephalyandobesityaseriesof17patients ‡A Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patients ‡9 1 | ||
| 919 | ‡a kosakiovergrowthsyndromeanovelpathogenicvariantinpdgfrbandexpansionofthephenotypeincludingcerebrovascularcomplications ‡A Kosaki overgrowth syndrome: a novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications ‡9 1 | ||
| 919 | ‡a chd8overgrowthsyndromeadetailedevaluationofanemergingovergrowthphenotypein27patients ‡A The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients ‡9 1 | ||
| 996 | ‡2 LC|no2008153298 | ||
| 996 | ‡2 J9U|987007354761105171 | ||
| 996 | ‡2 RERO|A023802375 | ||
| 996 | ‡2 LC|n 96001148 | ||
| 996 | ‡2 NDL|01065168 | ||
| 996 | ‡2 LC|nb2005009300 | ||
| 996 | ‡2 ISNI|000000003549964X | ||
| 996 | ‡2 SUDOC|085755532 | ||
| 996 | ‡2 ISNI|0000000069694750 | ||
| 996 | ‡2 SUDOC|175359261 | ||
| 996 | ‡2 ISNI|0000000394506549 | ||
| 996 | ‡2 PTBNP|1214302 | ||
| 996 | ‡2 NUKAT|n 2007086163 | ||
| 996 | ‡2 ISNI|0000000037852750 | ||
| 996 | ‡2 ISNI|0000000362204562 | ||
| 996 | ‡2 ISNI|0000000033376646 | ||
| 996 | ‡2 LC|no2024137590 | ||
| 996 | ‡2 LC|n 84208895 | ||
| 996 | ‡2 CAOONL|ncf10128195 | ||
| 996 | ‡2 LC|no2021006596 | ||
| 996 | ‡2 LC|no2015089201 | ||
| 996 | ‡2 LC|nb2016013989 | ||
| 996 | ‡2 J9U|987007271224205171 | ||
| 996 | ‡2 LC|no2010061011 | ||
| 996 | ‡2 ISNI|0000000038443115 | ||
| 996 | ‡2 LC|n 2005172281 | ||
| 996 | ‡2 LC|n 93086798 | ||
| 996 | ‡2 NII|DA16330718 | ||
| 996 | ‡2 J9U|987007383460405171 | ||
| 996 | ‡2 LC|nb2009009087 | ||
| 996 | ‡2 ISNI|0000000028572351 | ||
| 996 | ‡2 BIBSYS|90234192 | ||
| 996 | ‡2 LC|n 92003080 | ||
| 996 | ‡2 NII|DA09209863 | ||
| 996 | ‡2 ISNI|0000000032028877 | ||
| 997 | ‡a 0 0 lived 0 0 ‡9 1 |
