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K A Przylepa

Showing results (1-10 of 7) with videos related to

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Cancer Genetics and Cytogenetics|July 1, 1988
Chromosome breaks and fragile sites in leukemic bone marrow cellsK A Przylepa, S L Wenger
Nature Genetics|December 1, 1995
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricansG A Meyers, S J Orlow, I R Munro, et al.
Prenatal Diagnosis|December 17, 1997
Prenatal ultrasonographic and molecular diagnosis of Apert syndromeK Filkins, J F Russo, S Boehmer, 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.
Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.
American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.
American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Cancer Genetics and Cytogenetics|July 1, 1988
Chromosome breaks and fragile sites in leukemic bone marrow cellsK A Przylepa, S L Wenger
Nature Genetics|December 1, 1995
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricansG A Meyers, S J Orlow, I R Munro, et al.
Prenatal Diagnosis|December 17, 1997
Prenatal ultrasonographic and molecular diagnosis of Apert syndromeK Filkins, J F Russo, S Boehmer, 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.
Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.
American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.
American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.
Pageof 1