skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Base de dados/Biblioteca: Science Citation Index Expanded (Web of Science) remover xxx: xxx remover SpringerLink (Online service) remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Berglund, Agnethe ; Viuff, Mette Hansen ; Skakkebæk, Anne ; Chang, Simon ; Stochholm, Kirstine ; Gravholt, Claus Højbjerg

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
2
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)

Xu, Gefeng ; Huang, Tianqing ; Jin, Xian ; Cui, Cunhe ; Li, Depeng ; Sun, Cong ; Han, Ying ; Mu, Zhenbo

Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

Texto completo disponível

Citações Citado por
3
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
Material Type:
Artigo 		Adicionar ao Meu Espaço

Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX

Reish, Orit ; Berryman, Todd ; Cunningham, Thomas R ; Sher, Carron ; Oetting, William S

Chromosome research, 2004-01, Vol.12 (2), p.125-132 [Periódico revisado por pares]

Netherlands: Springer Nature B.V

Texto completo disponível

Citações Citado por
4
47,XXX females, sex chromosomes, and tooth crown structure
47,XXX females, sex chromosomes, and tooth crown structure
Material Type:
Artigo 		Adicionar ao Meu Espaço

47,XXX females, sex chromosomes, and tooth crown structure

Alvesalo, L ; Tammisalo, E ; Therman, E

Human genetics, 1987-12, Vol.77 (4), p.345-348 [Periódico revisado por pares]

Germany

Texto completo disponível

Citações Citado por
5
Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell lines
Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell lines
Material Type:
Artigo 		Adicionar ao Meu Espaço

Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell lines

PARTSCH, C.-J ; PANKAU, R ; SIPPELL, W. G ; TOLKSDORF, M

European journal of pediatrics, 1994-06, Vol.153 (6), p.451-455 [Periódico revisado por pares]

Heidelberg: Springer

Texto completo disponível

Citações Citado por
6
A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY
A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY
Material Type:
Artigo 		Adicionar ao Meu Espaço

A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY

VOGEL, W ; GROMPE, M ; STORZ, R ; PENTZ, S

Human genetics, 1984-01, Vol.66 (4), p.367-369 [Periódico revisado por pares]

Heidelberg: Springer

Texto completo disponível

Citações Citado por
7
Hormonal studies in a male with a 47,XXX chromosome constitution: comparison with the hormonal pattern of a 46,XX male and patients with Klinefelter's syndrome
Hormonal studies in a male with a 47,XXX chromosome constitution: comparison with the hormonal pattern of a 46,XX male and patients with Klinefelter's syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hormonal studies in a male with a 47,XXX chromosome constitution: comparison with the hormonal pattern of a 46,XX male and patients with Klinefelter's syndrome

Borghi, A ; Forti, G ; Fusi, S ; Bigozzi, U ; Giusti, G

Journal of endocrinological investigation, 1980-04, Vol.3 (2), p.163-168 [Periódico revisado por pares]

Italy

Texto completo disponível

Citações Citado por
8
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases

Lu, Xinran ; Wang, Chaohong ; Sun, Yuxiu ; Tang, Junxiang ; Tong, Keting ; Zhu, Jiansheng

Molecular cytogenetics, 2021-01, Vol.14 (1), p.1-1, Article 1 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
9
“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies
“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies
Material Type:
Artigo 		Adicionar ao Meu Espaço

“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies

Dennis, Anna ; Howell, Susan ; Cordeiro, Lisa ; Tartaglia, Nicole

Journal of genetic counseling, 2015-02, Vol.24 (1), p.88-103 [Periódico revisado por pares]

New York: Springer US

Texto completo disponível

Citações Citado por
10
The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes
The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes
Material Type:
Artigo 		Adicionar ao Meu Espaço

The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes

Martel, Rachel A. ; Blakemore, Jennifer K. ; Fino, M. Elizabeth

Journal of assisted reproduction and genetics, 2022-05, Vol.39 (5), p.1143-1153 [Periódico revisado por pares]

New York: Springer US

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (472)
  2. Revistas revisadas por pares (484)

Data de Publicação 

De até
Refinar
  1. Antes de1984  (13)
  2. 1984Até1995  (12)
  3. 1996Até2003  (21)
  4. 2004Até2012  (135)
  5. Após 2012  (310)
  6. Mais opções open sub menu

Idioma 

  1. Japonês  (53)
  2. Russo  (2)
  3. Norueguês  (1)
  4. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.