Coming together for blastogenesis [5]

American Journal of Medical Genetics

Volumn 117 A, Issue 3, 2003, Pages 309-

  Wilson, Golder N ^a,b  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF TEXAS AT DALLAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; CELL TYPE; CHROMOSOME 18; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; GENE IDENTIFICATION; HOLOPROSENCEPHALY; HUMAN; KIDNEY MALFORMATION; LETTER; LIMB MALFORMATION; LIVER DISEASE; LUNG MALFORMATION; LYMPHOCYTE TRANSFORMATION; MATERNAL DIABETES MELLITUS; NONHUMAN; PRIMITIVE STREAK; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SPLEEN DISEASE; SYNDROME VATER; TERATOGENESIS; TRISOMY 13; CHROMOSOME ABERRATION; ENCEPHALOCELE; FETUS DISEASE; GENETICS; MULTIPLE MALFORMATION SYNDROME; NOTE; PATHOLOGY;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; ENCEPHALOCELE; FETAL DISEASES; HOLOPROSENCEPHALY; HUMANS;

EID: 0042266865     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (7)

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4. Lubinsky M. 1986. Current concepts: VATER and other associations. Historical perspectives and modern interpretations. Am J Med Genet Suppl 2:9-16.
5. Opitz JM. 1982. The developmental field concept in clinical genetics. J Pediatr 101:805-809.
6. Opitz JM, Gilbert EF. 1982. CNS anomalies and the midline as a "developmental field". Am J Med Genet 12:443-455.
7. Wilson GN. 1996. A model for human situs determination. Laterality 1:315-329.