Novel mutations in prenatal diagnosis of primary microcephaly [1]

Prenatal Diagnosis

Volumn 26, Issue 10, 2006, Pages 989-

  Desir, Julie ^a   Abramowicz, Marc ^a   Tunca, Yusuf ^b  

^a ERASME HOSPITAL   (Belgium)

^b GULHANE SCHOOL OF MEDICINE   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CODON; EXON; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; LETTER; MICROCEPHALY; MORPHOMETRICS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

FEMALE; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MICROCEPHALY; MUTATION; NERVE TISSUE PROTEINS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 33750542340     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1536     Document Type: Letter

References (2)

1. Tunca Y, Vurucu S, Parma J, et al. 2006. Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data. Prenat Diagn 26(5): 449-453.
2. Woods CG, Bond J, Enard W. 2005. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. Am J Hum Genet 76(5): 717-728.