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Refinado por: Nome da Publicação: American Journal of Medical Genetics. Part A remover
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Noonan syndrome in diverse populations

Paul Kruszka Antonio R Porras; Yonit A Addissie; Angélica Moresco; Sofia Medrano; Gary T. K Mok; Gordon K. C Leung; Cedrik Tekendo-Ngongang; Annette Uwineza; Meow-Keong Thong; Premala Muthukumarasamy; Engela Honey; Ekanem N Ekure; Ogochukwu J Sokunbi; Nnenna Kalu; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Lisa M Vincent; Amber Love; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Anju Shukla; Katta M Girisha; Siddaramappa J Patil; Nirmala D Sirisena; Vajira H. W Dissanayake; C. Sampath Paththinige; Rupesh Mishra; Eva Klein-Zighelboim; Bertha E. Gallardo Jugo; Miguel Chávez Pastor; Hugo H Abarca-Barriga; Steven A Skinner; Eloise J Prijoles; Eben Badoe; Ashleigh D Gill; Vorasuk Shotelersuk; Patroula Smpokou; Monisha S Kisling; Carlos R Ferreira; Leon Mutesa; Andre Megarbane; Antonie D Kline; Amy Kimball; Emmy Okello; Peter Lwabi; Twalib Aliku; Emmanuel Tenywa; Nonglak Boonchooduang; Pranoot Tanpaiboon; Antonio Richieri-Costa; Ambroise Wonkam; Brian H. Y Chung; Roger E Stevenson; Marshall Summar; Kausik Mandal; Shubha R Phadke; María G Obregon; Marius G Linguraru; Maximilian Muenke

American Journal of Medical Genetics. Part A Hoboken v. 173, n. 9, p. 2323-2334, Sept. 2017

Hoboken 2017

Item não circula. Consulte sua biblioteca.(Acessar)

2
EEF1A2 pathogenic variant presenting in an infant with failure to thrive and frequent apneas requiring respiratory support
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EEF1A2 pathogenic variant presenting in an infant with failure to thrive and frequent apneas requiring respiratory support

Vogt, Lindsey M. ; Lorenzo, Melissa ; B. Prendergast, D'Arcy ; Jobling, Rebekah ; Gill, Peter J.

American journal of medical genetics. Part A, 2022-10, Vol.188 (10), p.3106-3109 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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3
Noonan syndrome in diverse populations
Material Type:
Artigo
Adicionar ao Meu Espaço

Noonan syndrome in diverse populations

Kruszka, Paul ; Porras, Antonio R. ; Addissie, Yonit A. ; Moresco, Angélica ; Medrano, Sofia ; Mok, Gary T. K. ; Leung, Gordon K. C. ; Tekendo‐Ngongang, Cedrik ; Uwineza, Annette ; Thong, Meow‐Keong ; Muthukumarasamy, Premala ; Honey, Engela ; Ekure, Ekanem N. ; Sokunbi, Ogochukwu J. ; Kalu, Nnenna ; Jones, Kelly L. ; Kaplan, Julie D. ; Abdul‐Rahman, Omar A. ; Vincent, Lisa M. ; Love, Amber ; Belhassan, Khadija ; Ouldim, Karim ; El Bouchikhi, Ihssane ; Shukla, Anju ; Girisha, Katta M. ; Patil, Siddaramappa J. ; Sirisena, Nirmala D. ; Dissanayake, Vajira H. W. ; Paththinige, C. Sampath ; Mishra, Rupesh ; Klein‐Zighelboim, Eva ; Gallardo Jugo, Bertha E. ; Chávez Pastor, Miguel ; Abarca‐Barriga, Hugo H. ; Skinner, Steven A. ; Prijoles, Eloise J. ; Badoe, Eben ; Gill, Ashleigh D. ; Shotelersuk, Vorasuk ; Smpokou, Patroula ; Kisling, Monisha S. ; Ferreira, Carlos R. ; Mutesa, Leon ; Megarbane, Andre ; Kline, Antonie D. ; Kimball, Amy ; Okello, Emmy ; Lwabi, Peter ; Aliku, Twalib ; Tenywa, Emmanuel ; Boonchooduang, Nonglak ; Tanpaiboon, Pranoot ; Richieri‐Costa, Antonio ; Wonkam, Ambroise ; Chung, Brian H. Y. ; Stevenson, Roger E. ; Summar, Marshall ; Mandal, Kausik ; Phadke, Shubha R. ; Obregon, María G. ; Linguraru, Marius G. ; Muenke, Maximilian

American journal of medical genetics. Part A, 2017-09, Vol.173 (9), p.2323-2334 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

Texto completo disponível

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Deste Autor:

  1. Patil, S
  2. Porras, A
  3. Love, A
  4. Shotelersuk, V
  5. Summar, M

Buscando em bases de dados remotas. Favor aguardar.