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1 .
Systemic and oral abnormalities in Kabuki syndrome: a case series
저자
by
Pinto, Lidiane Castro
;
Kokitsu-Nakata, Nancy Mizue
;
da Silva Dalben, Gisele
;
de Azevedo Silva, Lucas José
;
de Almeida, Ana Lúcia Pompéia Fraga
.
소스
In
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
May 2024 137(5):e91-e98
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7 . Academic Journal
Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review.
저자
by
Serigatto, Henrique Regonaschi
;
Kokitsu‐Nakata, Nancy Mizue
;
Vendramini‐Pittoli, Siulan
;
Tonello, Cristiano
;
Moura, Priscila Padilha
, et al.
소스
American Journal of Medical Genetics. Part A; Oct2023, Vol. 191 Issue 10, p2493-2507, 15p
Web of Science
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7 . Periodical
Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2
저자
by
Vendramini-Pittoli, Siulan
;
Candido-Souza, Rosana Maria
;
Quiezi, Rodrigo Gonçalves
;
Zechi-Ceide, Roseli Maria
;
Kokitsu-Nakata, Nancy Mizue
, et al.
소스
Journal of Pediatric Genetics; December 2020, Vol. 9 Issue: 4 p258-262, 5p
JCR 저널정보
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7 . Academic Journal
Clinical Genetic Study of 144 Patients With Nonsyndromic Hearing Loss.
저자
by
Kokitsu-Nakata, Nancy Mizue
;
Guion-Almeida, Maria Leine
;
Richieri-Costa, Antonio
.
소스
American Journal of Audiology
; Dec2004, Vol. 13 Issue 2, p99-103, 5p
EBSCOHost PDF
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5 . Academic Journal
Tratamento ortodôntico da agenesia de incisivos inferiores com aparelho de Herbst em um paciente sindrômico: follow up de 12 anos. (Portuguese)
저자
by
ALCA, Roxana Esmeralda Aparicio
;
SELANI, Vitória Piasentine
;
RIBEIRO, Tiago Turri de Castro
;
VAN DER LAAN, Helena Doneux
;
MASSARO, Camila
, et al.
소스
Universidade Estadual Paulista. Revista de Odontologia; 2023 Special Issue, Vol. 52, p266-266, 1p
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7 . Academic Journal
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect.
저자
by
Romanelli Tavares, Vanessa L
;
Gordon, Christopher T
;
Zechi-Ceide, Roseli M
;
Kokitsu-Nakata, Nancy Mizue
;
Voisin, Norine
, et al.
소스
European Journal of Human Genetics
. Apr2015, Vol. 23 Issue 4, p481-485. 5p.
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7 . Periodical
Multisystem Involvement in a Patient with a PTCH1 Mutation: Clinical and Imaging Findings
저자
by
Richieri-Costa, Antonio
;
Vendramini-Pittoli, Siulan
;
Kokitsu-Nakata, Nancy Mizue
;
Zechi-Ceide, Roseli Maria
;
Alvarez, Camila Wenceslau
, et al.
소스
Journal of Pediatric Genetics; June 2017, Vol. 6 Issue: 2 p103-106, 4p
JCR 저널정보
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7 . Academic Journal
Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome
저자
by
Kokitsu-Nakata, Nancy Mizue
;
Lourenço Petrin, Aline
;
Heard, Jason Paul
;
Vendramini-Pittoli, Siulan
;
Henkle, Laura E
, et al.
소스
American Journal Of Medical Genetics - A
. Aug 01, 2012 158A(8):2003-2008
Web of Science
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7 . Academic Journal
Saethre–Chotzen Phenotype With Learning Disability and Hyper IgE Phenotype in a Patient Due to Complex Chromosomal Rearrangement Involving Chromosomes 3 and 7
저자
by
Zechi-Ceide, Roseli Maria
;
Rodrigues, Melina Guerreiro
;
Jehee, Fernanda Sarquis
;
Kokitsu-Nakata, Nancy Mizue
;
Passos-Bueno, Maria Rita
, et al.
소스
American Journal Of Medical Genetics - A
. Jul 01, 2012 158A(7):1680-1685
Web of Science
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7 . Academic Journal
Auriculo–Condylar Syndrome. Confronting A Diagnostic Challenge
저자
by
Kokitsu–Nakata, Nancy Mizue
;
Zechi–Ceide, Roseli Maria
;
Vendramini–Pittoli, Siulan
;
Romanelli Tavares, Vanessa Luiza
;
Passos–Bueno, Maria Rita
, et al.
소스
American Journal Of Medical Genetics - A
. Jan 01, 2012 158A(1):59-65
Web of Science
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