Gollop T[Au] - Search Results

Year	Number of Results
1978	1
1980	2
1981	1
1982	2
1983	3
1984	2
1985	3
1987	3
1988	2
1990	1
1991	1
1992	1
2003	1
2004	1
2009	1
2010	3
2012	1
2018	1
2019	1
2020	1
2021	1
2024	0

1

Development of a comprehensive noninvasive prenatal test.

Malcher C, Yamamoto GL, Burnham P, Ezquina SAM, Lourenço NCV, Balkassmi S, Antonio DSM, Hsia GSP, Gollop T, Pavanello RC, Lopes MA, Bakker E, Zatz M, Bertola D, Vlaminck I, Passos-Bueno MR. Malcher C, et al. Among authors: gollop t. Genet Mol Biol. 2018 Jul/Sept.;41(3):545-554. doi: 10.1590/1678-4685-GMB-2017-0177. Epub 2018 Jul 16. Genet Mol Biol. 2018. PMID: 30043834 Free PMC article.

2

The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literature.

Pagnan NA, Gollop TR, Lederman H. Pagnan NA, et al. Among authors: gollop tr. Am J Med Genet. 1988 Feb;29(2):411-7. doi: 10.1002/ajmg.1320290224. Am J Med Genet. 1988. PMID: 3281460 Review.

3

The association between personal history and the outcomes of transobturator sling surgery.

Feitosa PDS, Colaço NHB, Barros CR, Gollop TR, Marchesini AC. Feitosa PDS, et al. Among authors: gollop tr. Rev Assoc Med Bras (1992). 2019 Jul 22;65(6):864-869. doi: 10.1590/1806-9282.65.6.864. Rev Assoc Med Bras (1992). 2019. PMID: 31340318 Free article.

4

The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.

Gollop TR, Fontes LR. Gollop TR, et al. Am J Med Genet. 1985 Sep;22(1):59-68. doi: 10.1002/ajmg.1320220106. Am J Med Genet. 1985. PMID: 3901752 Review.

5

Prenatal diagnosis of thalidomide syndrome.

Gollop TR, Eigier A, Guidugli Neto J. Gollop TR, et al. Prenat Diagn. 1987 May;7(4):295-8. doi: 10.1002/pd.1970070411. Prenat Diagn. 1987. PMID: 3295847

6

Urinary incontinence after vaginal delivery or cesarean section.

Borges JB, Guarisi T, Camargo AC, Gollop TR, Machado RB, Borges PC. Borges JB, et al. Among authors: gollop tr. Einstein (Sao Paulo). 2010 Jun;8(2):192-6. doi: 10.1590/S1679-45082010AO1543. Einstein (Sao Paulo). 2010. PMID: 26760002 Free article. English, Portuguese.

7

Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer.

Bandeira G, Rocha K, Lazar M, Ezquina S, Yamamoto G, Varela M, Takahashi V, Aguena M, Gollop T, Zatz M, Passos-Bueno MR, Krepischi A, Okamoto OK. Bandeira G, et al. Among authors: gollop t. Breast Cancer. 2021 Mar;28(2):346-354. doi: 10.1007/s12282-020-01165-1. Epub 2020 Sep 28. Breast Cancer. 2021. PMID: 32986223

8

X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families.

Visinoni AF, de Souza RL, Freire-Maia N, Gollop TR, Chautard-Freire-Maia EA. Visinoni AF, et al. Among authors: gollop tr. Am J Med Genet A. 2003 Sep 15;122A(1):51-5. doi: 10.1002/ajmg.a.20276. Am J Med Genet A. 2003. PMID: 12949972

9

Prenatal diagnosis of 48,XYY, +21 ascertained through ultrasound anomalies.

Gollop TR, Naccache NF, Auler-Bittencourt E, Hauschild D, Eigier A, Zveibil DK. Gollop TR, et al. Am J Med Genet. 1991 Apr 1;39(1):76-7. doi: 10.1002/ajmg.1320390116. Am J Med Genet. 1991. PMID: 1831009

10

Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophy.

Yamamoto LU, Gollop TR, Naccache NF, Pavanello RC, Zanoteli E, Zatz M, Vainzof M. Yamamoto LU, et al. Among authors: gollop tr. Diagn Mol Pathol. 2004 Sep;13(3):167-71. doi: 10.1097/01.pdm.0000124912.24194.d0. Diagn Mol Pathol. 2004. PMID: 15322429

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