Results
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Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. [electronic resource] by
- Kremer, H
- Kraaij, R
- Toledo, S P
- Post, M
- Fridman, J B
- Hayashida, C Y
- van Reen, M
- Milgrom, E
- Ropers, H H
- Mariman, E
Producer: 19950524
In:
Nature genetics vol. 9
Availability: No items available.
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5.
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Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family. [electronic resource] by
- Kremer, H
- Kuyt, L P
- van den Helm, B
- van Reen, M
- Leunissen, J A
- Hamel, B C
- Jansen, C
- Mariman, E C
- Frants, R R
- Padberg, G W
Producer: 19970108
In:
Human molecular genetics vol. 5
Availability: No items available.
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6.
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Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10. [electronic resource] by
- Van Der Zwaag, B
- Verzijl, H T F M
- Beltran-Valero De Bernabe, D
- Schuster, V L
- Van Bokhoven, H
- Kremer, H
- Van Reen, M
- Wichers, G H
- Brunner, H G
- Padberg, G W
Producer: 20020708
In:
Journal of medical genetics vol. 39
Availability: No items available.
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7.
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Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6. [electronic resource] by
- Ion, A
- Crosby, A H
- Kremer, H
- Kenmochi, N
- Van Reen, M
- Fenske, C
- Van Der Burgt, I
- Brunner, H G
- Montgomery, K
- Kucherlapati, R S
- Patton, M A
- Page, C
- Mariman, E
- Jeffery, S
Producer: 20001207
In:
Journal of medical genetics vol. 37
Availability: No items available.
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8.
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A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty. [electronic resource] by
- Kremer, H
- Martens, J W
- van Reen, M
- Verhoef-Post, M
- Wit, J M
- Otten, B J
- Drop, S L
- Delemarre-van de Waal, H A
- Pombo-Arias, M
- De Luca, F
- Potau, N
- Buckler, J M
- Jansen, M
- Parks, J S
- Latif, H A
- Moll, G W
- Epping, W
- Saggese, G
- Mariman, E C
- Themmen, A P
- Brunner, H G
Producer: 19990413
In:
The Journal of clinical endocrinology and metabolism vol. 84
Availability: No items available.
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9.
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Localization of the gene for Cowden disease to chromosome 10q22-23. [electronic resource] by
- Nelen, M R
- Padberg, G W
- Peeters, E A
- Lin, A Y
- van den Helm, B
- Frants, R R
- Coulon, V
- Goldstein, A M
- van Reen, M M
- Easton, D F
- Eeles, R A
- Hodgsen, S
- Mulvihill, J J
- Murday, V A
- Tucker, M A
- Mariman, E C
- Starink, T M
- Ponder, B A
- Ropers, H H
- Kremer, H
- Longy, M
- Eng, C
Producer: 19960809
In:
Nature genetics vol. 13
Availability: No items available.
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