Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes

Clinical Genetics

Volumn 74, Issue 2, 2008, Pages 145-154

  Menko, Fred H ^a   Kneepkens, C M F ^a   de Leeuw, N ^b   Peeters, E A J ^c   Van Maldergem, E ^d   Kamsteeg, E J ^b   Davidson, R ^e   Rozendaal, L ^a   Lasham, C A ^f   Peeters Scholte, C M P ^a   Jansweijer, M C ^g   Hilhorst Hofstee, Y ^h   Gille, J J P ^a   Heins, Y M ^a   Nieuwint, A W M ^a   Sistermans, E A ^a,b  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c MEDICAL CENTER HAAGLANDEN   (Netherlands)

^d UNIVERSITY OF LIÈGE   (Belgium)

^e Ferguson Smith Centre for Clinical Genetics   (United Kingdom)

^f Tergooi Hospitals ^*  (Netherlands)

^g ACADEMIC MEDICAL CENTER   (Netherlands)

^h LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

10q23; BMPR1A; Juvenile polyposis; PTEN

Indexed keywords

BONE MORPHOGENETIC PROTEIN RECEPTOR 1A; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ADOLESCENT; ADULT; ANEMIA; ARTICLE; CANCER STAGING; CASE REPORT; CHILD; CHROMOSOME 10Q; CHROMOSOME 10Q23; CHROMOSOME DELETION; CLINICAL FEATURE; COLON ADENOCARCINOMA; COLON RESECTION; COLONOSCOPY; COLORECTAL CANCER; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL MALFORMATION; CORRELATION ANALYSIS; DIARRHEA; DISEASE SEVERITY; FACE DYSMORPHIA; FEMALE; GASTROINTESTINAL ENDOSCOPY; GASTROINTESTINAL POLYPOSIS; GASTROINTESTINAL SYMPTOM; GENE DELETION; GENE INTERACTION; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; ILEOSTOMY; INFANTILE JUVENILE POLYP; JUVENILE POLYP; LIVER METASTASIS; MACROCEPHALY; MALE; MENTAL DEFICIENCY; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; RECTUM CANCER; SINGLE NUCLEOTIDE POLYMORPHISM;

ABNORMALITIES, MULTIPLE; AGE OF ONSET; BONE MORPHOGENETIC PROTEIN RECEPTORS, TYPE I; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 10; COLORECTAL NEOPLASMS; FEMALE; GASTROINTESTINAL DISEASES; HUMANS; INFANT; INFANT, NEWBORN; INTESTINAL POLYPOSIS; MALE; MENTAL RETARDATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; PTEN PHOSPHOHYDROLASE; SEQUENCE DELETION;

EID: 47149087382     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2008.01026.x     Document Type: Article

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