Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25.

Burkardt, Deepika D'Cunha; Rosenfeld, Jill A; Helgeson, Maria L; Angle, Brad; Banks, Valerie; Smith, Wendy E; Gripp, Karen W; Moline, Jessica; Moran, Rocio T; Niyazov, Dmitriy M; Stevens, Cathy A; Zackai, Elaine; Lebel, Robert Roger; Ashley, Douglas G; Kramer, Nancy; Lachman, Ralph S; Graham, John M

Burkardt, Deepika D'Cunha; Rosenfeld, Jill A; Helgeson, Maria L; Angle, Brad; Banks, Valerie; Smith, Wendy E; Gripp, Karen W; Moline, Jessica; Moran, Rocio T; Niyazov, Dmitriy M; Stevens, Cathy A; Zackai, Elaine; Lebel, Robert Roger; Ashley, Douglas G; Kramer, Nancy; Lachman, Ralph S; Graham, John M.

Affiliation

Burkardt DD; Medical Genetics Institute, Cedars Sinai Medical Center, Los Angeles, California, USA.

Am J Med Genet A ; 155A(6): 1336-51, 2011 Jun.

Article in En | MEDLINE | ID: mdl-21548129

Subject(s)

Abnormalities, Multiple/pathology; Chromosome Deletion; Chromosome Disorders/pathology; Chromosomes, Human, Pair 1/genetics; Face/abnormalities; Intellectual Disability/pathology; Phenotype; Abnormalities, Multiple/genetics; Adolescent; Child; Child, Preschool; Chromosome Disorders/genetics; Comparative Genomic Hybridization; Humans; In Situ Hybridization, Fluorescence; Infant; Intellectual Disability/genetics; Microarray Analysis; Syndrome; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Abnormalities, Multiple / Chromosomes, Human, Pair 1 / Chromosome Deletion / Chromosome Disorders / Face / Intellectual Disability Limits: Adolescent / Adult / Child / Child, preschool / Humans / Infant Language: En Journal: Am J Med Genet A Year: 2011 Document type: Article

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