(Q33561817)

28 July 2017

title

Intrauterine growth retardation associated with precocious puberty and sertoli cell hyperplasia (English)

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intrauterine growth restriction

28 July 2017

1 reference

1 reference

G Sabnis

4

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author name string

M B Lodish

1

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28 July 2017

L A Gartner

2

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28 July 2017

P Albini

3

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28 July 2017

A Brodie

5

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28 July 2017

J M Meck

6

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28 July 2017

A M Meloni-Ehrig

7

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28 July 2017

S Hill

8

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28 July 2017

E Tsilou

9

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28 July 2017

V A Valera

10

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28 July 2017

B A Walter

11

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28 July 2017

M J Merino

12

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28 July 2017

C A Stratakis

13

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28 July 2017

publication date

21 April 2010

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Hormone and Metabolic Research

28 July 2017

published in

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28 July 2017

volume

42

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28 July 2017

issue

9

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28 July 2017

page(s)

682-688

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The genetic aetiology of Silver-Russell syndrome

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

An immortalized human cell line bearing a PRKAR1A-inactivating mutation: effects of overexpression of the wild-type Allele and other protein kinase A subunits

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Cryptorchidism: classification, prevalence and long-term consequences

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Clinical significance of Ki-67 proliferation index in disease progression and prognosis of patients with resected colorectal carcinoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Chromosome 2 (2p16) abnormalities in Carney complex tumours

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences--a Children's Cancer Group study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Maternal uniparental disomy 7 in Silver-Russell syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Reevaluation of Russell-Silver syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Leiomyosarcoma in a patient with trisomy 8 mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Optic disc coloboma and localized chorioretinal defects in constitutional partial trisomy 8 mosaicism.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Prepubertal gynecomastia in Peutz-Jeghers syndrome: incomplete penetrance in a familial case and management with an aromatase inhibitor

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Gynecomastia and mucosal lentigines in an 8-year-old boy.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Comparison of single versus multiple dose regimens for the human chorionic gonadotropin stimulatory test

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Diploid-triploid mixoploidy: clinical and cytogenetic aspects

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412584

Aromatase expression in the human male

31 October 2018

1 reference

12 December 2020

Trisomy 8 mosaicism syndrome. Two cases demonstrating variability in phenotype

1 reference

12 December 2020

An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia

1 reference

12 December 2020

Chromosome analysis of parallel short-term cultures from four testicular germ-cell tumors

1 reference

12 December 2020

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

12 December 2020

ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS

1 reference

12 December 2020

Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH

1 reference

12 December 2020

Trisomy 8 as sole karyotypic aberration in an ovarian metastasizing Sertoli-Leydig cell tumor

1 reference

12 December 2020

Identifiers

DOI

10.1055/S-0030-1252021

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28 July 2017

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28 July 2017

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