Inherited (13;14) translocation and reproduction. Report on three families

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.

Clinical genetics·2014

A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability.

Clinical genetics·2007

Free sialic acid storage (Salla) disease in Sweden.

Acta paediatrica (Oslo, Norway : 1992)·2003

Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine families.

Prenatal diagnosis·2001

A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria.

Clinical genetics·2001

The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.

American journal of human genetics·2000

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Novel and recurrent TUBB8 variants cause irreversible meiotic spindle defects and refractory ART failure in Chinese women with oocyte maturation arrest.

Journal of assisted reproduction and genetics·2026

Novel Male Contraceptive Methods.

Nursing for women's health·2026

Recall and understanding of HIV-related counseling messages among progestin implant and injectable contraception users in Malawi.

AIDS care·2026

Three Concurrent Nonpalpable Nexplanon Implants in the Upper Arms Following Presumed Failed Insertions: A Case Report.

Case reports in obstetrics and gynecology·2026

Characterisation of seminal plasma-derived mediators involved in PMN evasion of ram spermatozoa in vitro.

Frontiers in immunology·2026

The impact of maternal hepatitis B virus infection on IVF/ICSI-assisted pregnancy outcomes: a propensity score-matched cohort study.

Frontiers in medicine·2026

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Inherited (13;14) translocation and reproduction. Report on three families

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Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.

A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability.

Free sialic acid storage (Salla) disease in Sweden.

Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine families.

A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria.

The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

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Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

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Recall and understanding of HIV-related counseling messages among progestin implant and injectable contraception users in Malawi.

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Inherited (13;14) translocation and reproduction. Report on three families

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