Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (Q33864953): Difference between revisions

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Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
label / astlabel / ast
 
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
label / nllabel / nl
 
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
description / ptdescription / pt
 
artigo científico (publicado na 1986)
description / csdescription / cs
 
vědecký článek
description / ardescription / ar
 
مقالة علمية
description / pt-brdescription / pt-br
 
artigo científico (publicado na 1986)
description / srdescription / sr
 
научни чланак
description / nldescription / nl
 
wetenschappelijk artikel
description / hydescription / hy
 
1986 թվականի մարտին հրատարակված գիտական հոդված
description / hudescription / hu
 
tudományos cikk
description / trdescription / tr
 
bilimsel makale
description / tgdescription / tg
 
мақолаи илмӣ
description / jadescription / ja
 
1986年の論文
description / bndescription / bn
 
১৯৮৬-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ
description / gldescription / gl
 
artigo científico
description / sr-eldescription / sr-el
 
naučni članak
description / eldescription / el
 
επιστημονικό άρθρο
description / svdescription / sv
 
vetenskaplig artikel
description / etdescription / et
 
teaduslik artikkel
description / yuedescription / yue
 
1986年論文
description / esdescription / es
 
artículo científico publicado en 1986
description / zh-cndescription / zh-cn
 
1986年论文
description / zh-mydescription / zh-my
 
1986年论文
description / pldescription / pl
 
artykuł naukowy
description / zh-hansdescription / zh-hans
 
1986年论文
description / ukdescription / uk
 
наукова стаття, опублікована в березні 1986
description / sqdescription / sq
 
artikull shkencor
description / dedescription / de
 
wissenschaftlicher Artikel
description / astdescription / ast
 
artículu científicu espublizáu en 1986
description / kadescription / ka
 
სამეცნიერო სტატია
description / dadescription / da
 
videnskabelig artikel (udgivet 1986)
description / nandescription / nan
 
1986 nî lūn-bûn
description / itdescription / it
 
articolo scientifico
description / zh-hantdescription / zh-hant
 
1986年論文
description / zh-modescription / zh-mo
 
1986年論文
description / videscription / vi
 
bài báo khoa học
description / nbdescription / nb
 
vitenskapelig artikkel
description / tldescription / tl
 
artikulong pang-agham
description / thdescription / th
 
บทความทางวิทยาศาสตร์
description / nndescription / nn
 
vitskapeleg artikkel
description / rudescription / ru
 
научная статья
description / fidescription / fi
 
tieteellinen artikkeli
description / frdescription / fr
 
article scientifique (publié 1986)
description / hedescription / he
 
מאמר מדעי
description / zh-twdescription / zh-tw
 
1986年論文
description / cadescription / ca
 
article científic
description / tg-cyrldescription / tg-cyrl
 
мақолаи илмӣ
description / sr-ecdescription / sr-ec
 
научни чланак
description / zh-hkdescription / zh-hk
 
1986年論文
description / eodescription / eo
 
scienca artikolo
description / skdescription / sk
 
vedecký článok
description / bgdescription / bg
 
научна статия
description / wuudescription / wuu
 
1986年论文
description / zhdescription / zh
 
1986年论文
description / ltdescription / lt
 
mokslinis straipsnis
description / zh-sgdescription / zh-sg
 
1986年论文
description / rodescription / ro
 
articol științific
description / ocdescription / oc
 
article scientific
description / kodescription / ko
 
1986년 논문
description / hywdescription / hyw
 
1986 թուականի Մարտին հրատարակուած գիտական յօդուած
description / fadescription / fa
 
مقالهٔ علمی
description / urdescription / ur
 
سائنسی مضمون
Property / titleProperty / title
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. (English)
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (English)
Property / cites work
 
Property / cites work: Deletions of chromosome 15 as a cause of the Prader-Willi syndrome / rank
 
Normal rank
Property / cites work: Deletions of chromosome 15 as a cause of the Prader-Willi syndrome / reference
 
Property / cites work
 
Property / cites work: The cytogenetic controversy in the Prader-Labhart-Willi syndrome / rank
 
Normal rank
Property / cites work: The cytogenetic controversy in the Prader-Labhart-Willi syndrome / reference
 
Property / cites work
 
Property / cites work: Prader-Willi syndrome: are there population differences? / rank
 
Normal rank
Property / cites work: Prader-Willi syndrome: are there population differences? / reference
 
Property / cites work
 
Property / cites work: Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases / rank
 
Normal rank
Property / cites work: Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases / reference
 
Property / cites work
 
Property / cites work: Translocations in Prader-Willi syndrome. / rank
 
Normal rank
Property / cites work: Translocations in Prader-Willi syndrome. / reference
 
Property / cites work
 
Property / cites work: Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome / rank
 
Normal rank
Property / cites work: Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome / reference
 
Property / cites work
 
Property / cites work: Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings. / rank
 
Normal rank
Property / cites work: Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings. / reference
 
Property / cites work
 
Property / cites work: Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases / rank
 
Normal rank
Property / cites work: Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases / reference
 
Property / cites work
 
Property / cites work: Prader-Willi syndrome in black females / rank
 
Normal rank
Property / cites work: Prader-Willi syndrome in black females / reference
 
Property / cites work
 
Property / cites work: The Prader-Willi syndrome: a study of 40 patients and a review of the literature / rank
 
Normal rank
Property / cites work: The Prader-Willi syndrome: a study of 40 patients and a review of the literature / reference
 
Property / cites work
 
Property / cites work: Parental origin of chromosome 15 deletion in Prader-Willi syndrome / rank
 
Normal rank
Property / cites work: Parental origin of chromosome 15 deletion in Prader-Willi syndrome / reference
 
Property / cites work
 
Property / cites work: The Prader-Labhart-Willi syndrome: review of the literature and report of nine cases / rank
 
Normal rank
Property / cites work: The Prader-Labhart-Willi syndrome: review of the literature and report of nine cases / reference
 
Property / cites work
 
Property / cites work: Hypogonadotropinism in Prader-Willi syndrome. Induction of puberty and sperm altogenesis by clomiphene citrate / rank
 
Normal rank
Property / cites work: Hypogonadotropinism in Prader-Willi syndrome. Induction of puberty and sperm altogenesis by clomiphene citrate / reference
 
Property / cites work
 
Property / cites work: Hypotonia, mental retardation, obesity, and cryptorchidism associated with dwarfism and diabetes in children / rank
 
Normal rank
Property / cites work: Hypotonia, mental retardation, obesity, and cryptorchidism associated with dwarfism and diabetes in children / reference
 
Property / cites work
 
Property / cites work: Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases. / rank
 
Normal rank
Property / cites work: Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases. / reference
 
Property / cites work
 
Property / cites work: High Resolution of Human Chromosomes / rank
 
Normal rank
Property / cites work: High Resolution of Human Chromosomes / reference
 
Property / cites work
 
Property / cites work: Growth, body composition, and development of obese and lean children / rank
 
Normal rank
Property / cites work: Growth, body composition, and development of obese and lean children / reference
 
Property / cites work
 
Property / cites work: The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature / rank
 
Normal rank
Property / cites work: The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature / reference
 
Property / cites work
 
Property / cites work: Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases / rank
 
Normal rank
Property / cites work: Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases / reference
 
Property / cites work
 
Property / cites work: Mental retardation associated with "balanced" chromosome rearrangements / rank
 
Normal rank
Property / cites work: Mental retardation associated with "balanced" chromosome rearrangements / reference
 
Property / cites work
 
Property / cites work: Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents / rank
 
Normal rank
Property / cites work: Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents / reference
 
Property / cites work
 
Property / cites work: Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13 / rank
 
Normal rank
Property / cites work: Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13 / reference
 
Property / cites work
 
Property / cites work: PRADER-WILLI SYNDROME IN BOY OF TEN WITH PREDIABETES. / rank
 
Normal rank
Property / cites work: PRADER-WILLI SYNDROME IN BOY OF TEN WITH PREDIABETES. / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992
retrieved: 29 October 2018
Timestamp+2018-10-29T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / cites work
 
Property / cites work: Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism / rank
 
Normal rank
Property / cites work: Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992
retrieved: 29 October 2018
Timestamp+2018-10-29T00:00:00Z
Timezone+00:00
CalendarGregorian
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Before0
After0
Property / cites work
 
Property / cites work: Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome / rank
 
Normal rank
Property / cites work: Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome / reference
 
stated in: PubMed Central
reference URL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992
retrieved: 29 October 2018
Timestamp+2018-10-29T00:00:00Z
Timezone+00:00
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Precision1 day
Before0
After0
Property / cites work
 
Property / cites work: Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population / rank
 
Normal rank
Property / cites work: Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
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Precision1 day
Before0
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based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: High-resolution bands in human fibroblast chromosomes induced by actinomycin D / rank
 
Normal rank
Property / cites work: High-resolution bands in human fibroblast chromosomes induced by actinomycin D / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome / rank
 
Normal rank
Property / cites work: Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Parental origin of de novo chromosome rearrangements / rank
 
Normal rank
Property / cites work: Parental origin of de novo chromosome rearrangements / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Prader--Willi syndrome associated with an interstitial deletion of chromosome 15 / rank
 
Normal rank
Property / cites work: Prader--Willi syndrome associated with an interstitial deletion of chromosome 15 / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
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Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Benign congenital hypotonia with chromosomal anomaly / rank
 
Normal rank
Property / cites work: Benign congenital hypotonia with chromosomal anomaly / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: A simple reproducible method for prometaphase chromosome analysis / rank
 
Normal rank
Property / cites work: A simple reproducible method for prometaphase chromosome analysis / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
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Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Roentgenographic Manifestations of the Prader-Willi Syndrome / rank
 
Normal rank
Property / cites work: Roentgenographic Manifestations of the Prader-Willi Syndrome / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
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Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Prader-Willi syndrome associated with inversion of chromosome 15 / rank
 
Normal rank
Property / cites work: Prader-Willi syndrome associated with inversion of chromosome 15 / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence / rank
 
Normal rank
Property / cites work: Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/3953677
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / language of work or name
 
Property / language of work or name: English / rank
 
Normal rank

Latest revision as of 21:40, 17 April 2022

scientific article
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English
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
scientific article

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    Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (English)

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