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Nederlands Tijdschrift Voor Geneeskunde
|
December 1, 2018
[Whole Exome Sequencing in daily practice: the possibilities and impossibilities of this diagnostic test]
Arjan Bouman, Alice S Brooks, Marjon A van Slegtenhorst
International Journal of Pediatric Otorhinolaryngology
|
May 23, 2015
JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance
Hans L J Hoeve, Alice S Brooks, Liesbeth S Smit
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
November 25, 2003
Association of congenital diaphragmatic hernia with limb-reduction defects
Marieke F van Dooren, Alice S Brooks, Dick Tibboel, et al.
Nephron
|
September 14, 2018
Diagnosing Alport Syndrome: Lessons from the Pediatric Ward
Paul Vos, Robert Zietse, Michel van Geel, et al.
Clinical Dysmorphology
|
May 11, 2002
Kabuki syndrome: a review study of three hundred patients
Marja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
Clinical Dysmorphology
|
May 11, 2002
Congenital diaphragmatic hernia in a female patient with craniofrontonasal syndrome
Alice S Brooks, Marieke van Dooren, Jeannette Hoogeboom, et al.
Clinical Dysmorphology
|
June 9, 2006
Two brothers with Goldberg-Shprintzen syndrome
Helen R Murphy, Melanie J Carver, Alice S Brooks, et al.
Pediatric Neurology
|
March 15, 2011
Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities
Daniela Q C M Barge-Schaapveld, Alice S Brooks, Maarten H Lequin, et al.
Journal of the American Society of Nephrology : JASN
|
July 16, 2017
A Missense Mutation in the Extracellular Domain of <i>α</i>ENaC Causes Liddle Syndrome
Mahdi Salih, Ivan Gautschi, Miguel X van Bemmelen, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2012
Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4
Judith M A Verhagen, Jan G Huijmans, Monique Williams, et al.
Page
of 7
Search research articles
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Showing results (1-10 of 62) with videos related to
Sort By:
Page
of 7
Nederlands Tijdschrift Voor Geneeskunde
|
December 1, 2018
[Whole Exome Sequencing in daily practice: the possibilities and impossibilities of this diagnostic test]
Arjan Bouman, Alice S Brooks, Marjon A van Slegtenhorst
International Journal of Pediatric Otorhinolaryngology
|
May 23, 2015
JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance
Hans L J Hoeve, Alice S Brooks, Liesbeth S Smit
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
November 25, 2003
Association of congenital diaphragmatic hernia with limb-reduction defects
Marieke F van Dooren, Alice S Brooks, Dick Tibboel, et al.
Nephron
|
September 14, 2018
Diagnosing Alport Syndrome: Lessons from the Pediatric Ward
Paul Vos, Robert Zietse, Michel van Geel, et al.
Clinical Dysmorphology
|
May 11, 2002
Kabuki syndrome: a review study of three hundred patients
Marja W Wessels, Alice S Brooks, Jeannette Hoogeboom, et al.
Clinical Dysmorphology
|
May 11, 2002
Congenital diaphragmatic hernia in a female patient with craniofrontonasal syndrome
Alice S Brooks, Marieke van Dooren, Jeannette Hoogeboom, et al.
Clinical Dysmorphology
|
June 9, 2006
Two brothers with Goldberg-Shprintzen syndrome
Helen R Murphy, Melanie J Carver, Alice S Brooks, et al.
Pediatric Neurology
|
March 15, 2011
Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities
Daniela Q C M Barge-Schaapveld, Alice S Brooks, Maarten H Lequin, et al.
Journal of the American Society of Nephrology : JASN
|
July 16, 2017
A Missense Mutation in the Extracellular Domain of <i>α</i>ENaC Causes Liddle Syndrome
Mahdi Salih, Ivan Gautschi, Miguel X van Bemmelen, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2012
Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4
Judith M A Verhagen, Jan G Huijmans, Monique Williams, et al.
Page
of 7