Search details
1.
4.3-Mb triplication of 4q32.1-q32.2: report of a family through two generations.
Am J Med Genet A
; 149A(10): 2274-9, 2009 Oct.
Article
in English
| MEDLINE | ID: mdl-19764020
2.
Interstitial deletion of 1p22.2p31.1 and medium-chain acyl-CoA dehydrogenase deficiency in a patient with global developmental delay.
Am J Med Genet A
; 146A(12): 1581-6, 2008 Jun 15.
Article
in English
| MEDLINE | ID: mdl-18478588
3.
Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.
Pediatr Blood Cancer
; 50(5): 1052-3, 2008 May.
Article
in English
| MEDLINE | ID: mdl-18213712
4.
Association of the t(12;22)(q13;q12) EWS/ATF1 rearrangement with polyphenotypic round cell sarcoma of bone: a case report.
Am J Surg Pathol
; 29(12): 1673-9, 2005 Dec.
Article
in English
| MEDLINE | ID: mdl-16327442
5.
A der(19)t(12;19)(q12;p13.3) in a case of pediatric acute leukemia with unusual immunophenotype.
Cancer Genet Cytogenet
; 157(2): 164-8, 2005 Mar.
Article
in English
| MEDLINE | ID: mdl-15721640
6.
Peripheral medulloepithelioma: an immunohistochemical, ultrastructural, and cytogenetic study of a rare, chemotherapy-sensitive, pediatric tumor.
Am J Surg Pathol
; 27(7): 1008-12, 2003 Jul.
Article
in English
| MEDLINE | ID: mdl-12826895
7.
An active ring X and haploinsufficiency of SHOX contribute to short stature, congenital anomalies, and developmental delay in a female.
Am J Med Genet
; 113(3): 279-85, 2002 Dec 01.
Article
in English
| MEDLINE | ID: mdl-12439897
8.
Genetic analysis of patients with the Saethre-Chotzen phenotype.
Am J Med Genet
; 110(2): 136-43, 2002 Jun 15.
Article
in English
| MEDLINE | ID: mdl-12116251
9.
Detecting rearrangements in children using subtelomeric FISH and SKY.
Am J Med Genet
; 107(4): 267-74, 2002 Feb 01.
Article
in English
| MEDLINE | ID: mdl-11840482
10.
Array-based genomic delineation of a familial duplication 11q14.1-q22.1 associated with recurrent depression.
Am J Med Genet B Neuropsychiatr Genet
; 141B(3): 214-9, 2006 Apr 05.
Article
in English
| MEDLINE | ID: mdl-16526031
11.
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
Am J Med Genet A
; 140(5): 509-14, 2006 Mar 01.
Article
in English
| MEDLINE | ID: mdl-16470794
12.
Malignant hematological disorders in children with Wolf-Hirschhorn syndrome.
Am J Med Genet A
; 119A(2): 194-9, 2003 Jun 01.
Article
in English
| MEDLINE | ID: mdl-12749063
13.
Intrascrotal lipoblastoma with a complex karyotype: a case report and review of the literature.
Arch Pathol Lab Med
; 128(7): 797-800, 2004 Jul.
Article
in English
| MEDLINE | ID: mdl-15214818
14.
Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma.
Am J Med Genet A
; 120A(1): 105-9, 2003 Jul 01.
Article
in English
| MEDLINE | ID: mdl-12794701
15.
Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.
Genomics
; 79(2): 186-96, 2002 Feb.
Article
in English
| MEDLINE | ID: mdl-11829489
16.
Human chromosome 7: DNA sequence and biology.
Science
; 300(5620): 767-72, 2003 May 02.
Article
in English
| MEDLINE | ID: mdl-12690205
17.
Response to correspondence from Gripp et al.-"clinical and molecular diagnosis should be consistent".
Am J Med Genet A
; 122A(1): 91, 2003 Sep 15.
Article
in English
| MEDLINE | ID: mdl-12949981
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