Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2

Laurence Faivre; André Megarbane; Valérie CORMIER-DAIRE; Abdulrahman Alswaid; Louise Zylberberg; Noura Aldohayan; Ana Belinda CAMPOS-XAVIER; Delphine Bacq; Laurence LEGEAI-MALLET; Jacky Bonaventure; Arnold Munnich

doi:10.1007/s00439-002-0689-3

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Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2

Journal article

Peer reviewed

Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2

Laurence Faivre, André Megarbane, Valérie CORMIER-DAIRE, Abdulrahman Alswaid, Louise Zylberberg, Noura Aldohayan, Ana Belinda CAMPOS-XAVIER, Delphine Bacq, Laurence LEGEAI-MALLET, Jacky Bonaventure, …

Human genetics, Vol.110(4), pp.366-370

01/04/2002

DOI: https://doi.org/10.1007/s00439-002-0689-3

PMID: 11941487

Abstract

Biological and medical sciences

Classical genetics, quantitative genetics, hybrids

Complex syndromes

Fundamental and applied biological sciences. Psychology

Genetics of eukaryotes. Biological and molecular evolution

Human

Medical genetics

Medical sciences

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Title: Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2
Creators - without role: Laurence Faivre - Inserm
André Megarbane - Saint Joseph University
Valérie CORMIER-DAIRE - Inserm
Abdulrahman Alswaid - Riyadh Armed Forces Hospital
Louise Zylberberg - Délégation Paris 7
Noura Aldohayan - Riyadh Armed Forces Hospital
Ana Belinda CAMPOS-XAVIER - Hôpital Necker-Enfants Malades
Delphine Bacq - National Center of Human Genomics Research
Laurence LEGEAI-MALLET - Hôpital Necker-Enfants Malades
Jacky Bonaventure - Hôpital Necker-Enfants Malades
Arnold Munnich - Hôpital Necker-Enfants Malades
Publication Details: Human genetics, Vol.110(4), pp.366-370
Publisher: Springer
Identifiers: 9920812908331
Academic Unit: King Abdulaziz University; King Saud Bin Abdulaziz University for Health Sciences
Language: English
Resource Type: Journal article