Latest papers

Robust age at onset linkage analysis in nuclear families.

Teething symptoms in the first year of life and associated factors: a cohort study.

The Residual Parent to Come: on the need for parental expertise and advice.

Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2.

How personal is the political? Democratic revolution and fertility decline.

Long-term survival after HLA-haploidentical SCT from noninherited maternal antigen-mismatched family donors: impact of chronic GVHD.

3q29 microdeletion: A mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs

Refusal of treatment--the need for better communication.

[Female doctors in the early history of European medicine].

Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9.

Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: When should IRF6 mutational screening be done?

Familial odontoid hypoplasia

van den Ende-Gupta syndrome: Evidence for genetic heterogeneity

MTHFR 677TT alone and IRF6 820GG together with MTHFR 677CT, but not MTHFR A1298C, are risks for nonsyndromic cleft lip with or without cleft palate in an Indian population.

Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome.

Sex ratio shift in offspring of male fixed-wing naval aviation officers.

Risk factors for type 2 diabetes in a sixth- grade multiracial cohort: the HEALTHY study.

Depression and quality of life for women in single-parent and nuclear families.

Growing rejection of female genital cutting among women of reproductive age in Amhara, Ethiopia

Diabetic subjects diagnosed through the Diabetes Prevention Trial-Type 1 (DPT-1) are often asymptomatic with normal A1C at diabetes onset.