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A Shanske

Showing results (11-20 of 18) with videos related to

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American Journal of Medical Genetics|March 15, 1993
Craniofacial, limb, and abdominal anomalies in a distinct syndrome: relation to the spectrum of Pfeiffer syndrome type 3C M Barone, R Marion, A Shanske, et al.
American Journal of Medical Genetics|January 23, 1999
Deletion of the pseudoautosomal region in a male with a unique Y;13 translocation and short statureA Shanske, J Ellison, P Vuguin, et al.
American Journal of Medical Genetics|July 23, 1998
Normal adaptive function with learning disability in duplication 8p including band p22S S Sklower Brooks, M Genovese, H Gu, et al.
American Journal of Human Genetics|November 30, 2000
AT-rich palindromes mediate the constitutional t(11;22) translocationL Edelmann, E Spiteri, K Koren, et al.
American Journal of Human Genetics|March 3, 1999
Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11B Funke, L Edelmann, N McCain, et al.
Prenatal Diagnosis|July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studiesL Y Hsu, S Kaffe, E C Jenkins, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
Academic Pediatrics|November 4, 2023
Impairment Types and Combinations Among Adolescents and Young Adults with Disabilities: Colorado 2014-2018Alyna T Chien, Sarah J Spence, Megumi J Okumura, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
American Journal of Medical Genetics|March 15, 1993
Craniofacial, limb, and abdominal anomalies in a distinct syndrome: relation to the spectrum of Pfeiffer syndrome type 3C M Barone, R Marion, A Shanske, et al.
American Journal of Medical Genetics|January 23, 1999
Deletion of the pseudoautosomal region in a male with a unique Y;13 translocation and short statureA Shanske, J Ellison, P Vuguin, et al.
American Journal of Medical Genetics|July 23, 1998
Normal adaptive function with learning disability in duplication 8p including band p22S S Sklower Brooks, M Genovese, H Gu, et al.
American Journal of Human Genetics|November 30, 2000
AT-rich palindromes mediate the constitutional t(11;22) translocationL Edelmann, E Spiteri, K Koren, et al.
American Journal of Human Genetics|March 3, 1999
Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11B Funke, L Edelmann, N McCain, et al.
Prenatal Diagnosis|July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studiesL Y Hsu, S Kaffe, E C Jenkins, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
Academic Pediatrics|November 4, 2023
Impairment Types and Combinations Among Adolescents and Young Adults with Disabilities: Colorado 2014-2018Alyna T Chien, Sarah J Spence, Megumi J Okumura, et al.
Pageof 2